KEELER AMOILS ACULL CRYO OPHTHALMIC UNIT— 510(k) K801418

Name: FDA 510(k) clearance K801418
Creator: U.S. Food and Drug Administration
Published: 1980-07-21

Substantially Equivalent

Keeler Optical Products , Ltd.

FDA 510(k) clearance K801418 for KEELER AMOILS ACULL CRYO OPHTHALMIC UNIT, Substantially Equivalent on 1980-07-21. Applicant: Keeler Optical Products , Ltd.. Device class: 2.

Clearance details

Applicant: Keeler Optical Products , Ltd.
Product code: Code HPS
Device class: Class 2
Regulation: 21 CFR 886.4170
Advisory panel: Ophthalmic
Date received: 1980-06-17
Decision date: 1980-07-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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