MEDPOR OCULAR SCREW AND ACCEOSSORIES— 510(k) K971583

Name: FDA 510(k) clearance K971583
Creator: U.S. Food and Drug Administration
Published: 1997-06-30

Substantially Equivalent

Porex Technologies Corp.

FDA 510(k) clearance K971583 for MEDPOR OCULAR SCREW AND ACCEOSSORIES, Substantially Equivalent on 1997-06-30. Applicant: Porex Technologies Corp.. Device class: 2.

Clearance details

Applicant: Porex Technologies Corp.
Product code: Code MQU
Device class: Class 2
Regulation: 21 CFR 886.3320
Advisory panel: Ophthalmic
Date received: 1997-04-30
Decision date: 1997-06-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fairburn, GA, US

Download summary PDF View on FDA.gov ↗

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