MODIFIED SITE DIAPHRAGM CASSETTE FOR OPHTHALMICS— 510(k) K922996

Name: FDA 510(k) clearance K922996
Creator: U.S. Food and Drug Administration
Published: 1992-07-27

Substantially Equivalent

Chiron Vision Corp.

FDA 510(k) clearance K922996 for MODIFIED SITE DIAPHRAGM CASSETTE FOR OPHTHALMICS, Substantially Equivalent on 1992-07-27. Applicant: Chiron Vision Corp.. Device class: 1.

Clearance details

Applicant: Chiron Vision Corp.
Product code: Code KYG
Device class: Class 1
Regulation: 21 CFR 886.4360
Advisory panel: Ophthalmic
Date received: 1992-06-22
Decision date: 1992-07-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Horsham, PA, US

Download summary PDF View on FDA.gov ↗

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