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Company K
Results: 1357

#	Item
991	MAR[removed]SonoScape Company LTD K; &Y SS1-8000 Mobile Digital Color Doppler Ultrasound System Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2011-04-25 00:30:19 Medical equipment Acoustics Medical ultrasonography Ultrasound Radiology Doppler Mindray Medical International Limited Ultrasound research interface Medicine Medical ultrasound Medical physics
992	510(k) Summary Date Prepared: Company: Contact: Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2013-02-06 08:16:56 Food law Medical equipment Pharmaceuticals policy Medical device Medical technology Premarket approval Center for Devices and Radiological Health Federal Food Drug and Cosmetic Act Title 21 of the Code of Federal Regulations Medicine Health Food and Drug Administration
993	BDO Seidman, LLP Accountants and Consultants 330 Madison Ave. New York, NY[removed]Telephone: ([removed] Add to Reading List Source URL: www.sec.gov Language: English - Date: 2005-10-31 14:45:44 Auditing Form 10-K Corporate governance United States corporate law Sarbanes–Oxley Act Finance Securities Exchange Act Public company Law United States securities law SEC filings Business
994	510(k) Summary February 27, [removed]Company: Contact: Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2013-09-13 12:40:14 Food law Surgery Stereotactic surgery Surgical oncology Medical device Medtronic Computer-assisted surgery Federal Food Drug and Cosmetic Act Premarket approval Medicine Food and Drug Administration Neurosurgery
995	K1136 JAN[removed]Section 5: 510(k) Summary Submitted by: The Procter & Gamble Company Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2012-02-27 00:32:15 Technology Feminine hygiene Personal hygiene products Food law Tampon Pharmaceuticals policy Rely Medical device Premarket approval Medicine Health Food and Drug Administration
996	JN 62012o 510(k) SummaryJA Submitter information Company name Establishment registration number Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2012-02-27 00:31:02 Food and Drug Administration Food law Medical equipment Implants Pharmaceuticals policy Medical device Federal Food Drug and Cosmetic Act Premarket approval Title 21 of the Code of Federal Regulations Medicine Health Medical technology
997	510(K) Summary: REVLOK Tm Fenestrated Screw System Company: Contact: Globus Medical Inc. Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2011-08-29 00:29:54 Implants Neurosurgery Skeletal system Vertebral fixation Spondylolisthesis Scoliosis Polyaxial screw Kyphosis Degenerative disc disease Medicine Orthopedic surgery Vertebral column
998	K13 1296 Page 1 of[removed]k) Summary Company Name: Wenzel Spine, Inc. Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2013-10-09 09:32:41 Vertebral column PLIF Spondylolisthesis Medical device Federal Food Drug and Cosmetic Act Degenerative disc disease Human vertebral column Premarket approval Center for Devices and Radiological Health Medicine Food and Drug Administration Health
999	NOV 510(k) Summary Company Ethicon Endo-Surgery, LLC Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2011-12-26 00:34:14 Surgery Endoscopy Surgical oncology Electrosurgery Laparoscopic surgery Ethicon Endo-Surgery Medical device Hysterectomy Center for Devices and Radiological Health Medicine Food and Drug Administration Food law
1000	510(k) Summary (April 5, 2012): Company: Elsertech, LLCAP Contact: Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2012-05-28 00:33:46 Food law Neurosurgery Orthopedic surgery Spinal fusion Medical device Spondylolisthesis Center for Devices and Radiological Health Degenerative disc disease Premarket approval Medicine Food and Drug Administration Vertebral column

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