NEVYAS AUTOPRESS EYE COMPRESSOR— 510(k) K792255

Name: FDA 510(k) clearance K792255
Creator: U.S. Food and Drug Administration
Published: 1979-12-11

Substantially Equivalent

Keeler Optical Products , Ltd.

FDA 510(k) clearance K792255 for NEVYAS AUTOPRESS EYE COMPRESSOR, Substantially Equivalent on 1979-12-11. Applicant: Keeler Optical Products , Ltd.. Device class: 2.

Clearance details

Applicant: Keeler Optical Products , Ltd.
Product code: Code LCC
Device class: Class 2
Regulation: 21 CFR 886.4610
Advisory panel: Ophthalmic
Date received: 1979-11-09
Decision date: 1979-12-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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