K[removed]Page I of[removed]k) Summary AribroCare® Corporation TURBINATORTM WAND

First Page		Document Content
Date: 2013-08-06 11:27:47 Medical device Premarket approval Title 21 of the Code of Federal Regulations Center for Devices and Radiological Health Quality management system Electrosurgery Wand Medicine Health Food and Drug Administration		K[removed]Page I of[removed]k) Summary AribroCare® Corporation TURBINATORTM WAND Add to Reading List Source URL: www.accessdata.fda.gov Download Document from Source Website File Size: 125,20 KB Share Document on Facebook

	Microsoft PowerPoint - ditto DocID: 1gc7K - View Document
	Microsoft PowerPoint - ditto DocID: 1g6Me - View Document
	Federal Register / Vol. 80, NoWednesday, May 6, Notices Submit electronic comments on the draft guidance to http:// www.regulations.gov. Submit written comments to the Division of Dockets Management (HFA– DocID: 1aGhA - View Document
	This document is scheduled to be published in the Federal Register onand available online at http://federalregister.gov/a, and on FDsys.govP DEPARTMENT OF HEALTH AND HUMAN SERVICES DocID: 1akUI - View Document
	CLEAN version with no appendices DocID: 1ahmv - View Document