DIOPTRON III AUTOREFRACTOR— 510(k) K801906

Name: FDA 510(k) clearance K801906
Creator: U.S. Food and Drug Administration
Published: 1980-08-27

Substantially Equivalent

Coherent Medical Division

FDA 510(k) clearance K801906 for DIOPTRON III AUTOREFRACTOR, Substantially Equivalent on 1980-08-27. Applicant: Coherent Medical Division. Device class: 1.

Clearance details

Applicant: Coherent Medical Division
Product code: Code HKO
Device class: Class 1
Regulation: 21 CFR 886.1760
Advisory panel: Ophthalmic
Date received: 1980-08-11
Decision date: 1980-08-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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