INSTRUMENTS, OVERREFRACTION SYSTEM— 510(k) K782096

Name: FDA 510(k) clearance K782096
Creator: U.S. Food and Drug Administration
Published: 1979-01-26

Substantially Equivalent

Zeiss Humphrey System

FDA 510(k) clearance K782096 for INSTRUMENTS, OVERREFRACTION SYSTEM, Substantially Equivalent on 1979-01-26. Applicant: Zeiss Humphrey System. Device class: 1.

Clearance details

Applicant: Zeiss Humphrey System
Product code: Code HLM
Device class: Class 1
Regulation: 21 CFR 886.1425
Advisory panel: Ophthalmic
Date received: 1978-12-18
Decision date: 1979-01-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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K930445 — MARCO LM-770 DIGITAL PROJECTION LENSMETER1993-06-21

More clearances from Zeiss Humphrey System

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K923348 — OPHTHALMIC A/B SCAN SYSTEM, MODEL 835 -- MODIFIED1992-12-10
K852639 — HUMPHREY FIELD ANALYZER MODEL 6301985-09-18
K852638 — HUMPHREY IMAGE ANALYZER MODEL 1101985-08-12

Data sourced from openFDA. This site is unofficial and independent of the FDA.