DeviceClearance

OMNI F.T. LATEX EXAMINATION GLOVE, POWDERED— 510(k) K973134

Substantially Equivalent

Omnigrace , Ltd.

FDA 510(k) clearance K973134 for OMNI F.T. LATEX EXAMINATION GLOVE, POWDERED, Substantially Equivalent on 1997-11-06. Applicant: Omnigrace , Ltd..

Clearance details

Applicant
Omnigrace , Ltd.
Product code
Code LYY
Advisory panel
General Hospital
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Canton, OH, US
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