MEDPOR OCULAR PEG SYSTEM AND ACCESSORIES— 510(k) K960859

Name: FDA 510(k) clearance K960859
Creator: U.S. Food and Drug Administration
Published: 1996-05-29

Substantially Equivalent

Porex Technologies Corp. of Georgia

FDA 510(k) clearance K960859 for MEDPOR OCULAR PEG SYSTEM AND ACCESSORIES, Substantially Equivalent on 1996-05-29. Applicant: Porex Technologies Corp. of Georgia. Device class: 2.

Clearance details

Applicant: Porex Technologies Corp. of Georgia
Product code: Code HPZ
Device class: Class 2
Regulation: 21 CFR 886.3320
Advisory panel: Ophthalmic
Date received: 1996-03-01
Decision date: 1996-05-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fairburn, GA, US

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