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Food law / Medical equipment / Ethicon Inc. / Johnson & Johnson / Premarket approval / Medical device / Alginate dressing / Federal Food / Drug / and Cosmetic Act / Center for Devices and Radiological Health / Medicine / Health / Food and Drug Administration


Document Date: 2003-03-14 10:05:44

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City

Exeter / Somerville / /

Company

Westaim Biomedical Inc / Johnson & Johnson Medical Limited / Ethicon Inc. / Wound Management Worldwide / /

/

Event

Natural Disaster / FDA Phase / /

IndustryTerm

announcements concerning your device / manufacturing practice requirements / manufacturing practice / Internet address http /

MedicalCondition

pressure ulcers / infection / venous ulcers / /

Organization

Food and Drug Administration / office of Compliance / United States Food and Drug Administration's Center for Devices and Radiological Health / office of Device Evaluation / Division of General / Device Evaluation Center for Devices / Division of Ethicon / Neurological Devices Office / Division of Small Manufacturers / International and Consumer Assistance / DEPARTMENT OF HEALTH / /

Person

Patricia Flood / Celia M. Witten / Restorative / /

/

Position

Senior Project Manager / Regulatory Affairs / Manager / Regulatory Affairs Johnson & Johnson / Project Manager / Regulatory Affairs / Director / physician / /

Product

26r7l02 8 Device Classification Antimicrobial / Federal Food / /

ProvinceOrState

New Jersey / /

Technology

radiation / /

URL

http /

SocialTag