AUTOKERATOMETER, INSTRUMENT— 510(k) K781994

Name: FDA 510(k) clearance K781994
Creator: U.S. Food and Drug Administration
Published: 1979-02-12

Substantially Equivalent

Zeiss Humphrey System

FDA 510(k) clearance K781994 for AUTOKERATOMETER, INSTRUMENT, Substantially Equivalent on 1979-02-12. Applicant: Zeiss Humphrey System. Device class: 1.

Clearance details

Applicant: Zeiss Humphrey System
Product code: Code HLQ
Device class: Class 1
Regulation: 21 CFR 886.1350
Advisory panel: Ophthalmic
Date received: 1978-11-29
Decision date: 1979-02-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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