ALLERGAN HUMPHREY AUTO-REFRACTOR, MODELS 525 & 540— 510(k) K871611

Name: FDA 510(k) clearance K871611
Creator: U.S. Food and Drug Administration
Published: 1987-05-18

Substantially Equivalent

Allergan Humphrey

FDA 510(k) clearance K871611 for ALLERGAN HUMPHREY AUTO-REFRACTOR, MODELS 525 & 540, Substantially Equivalent on 1987-05-18. Applicant: Allergan Humphrey. Device class: 1.

Clearance details

Applicant: Allergan Humphrey
Product code: Code HKO
Device class: Class 1
Regulation: 21 CFR 886.1760
Advisory panel: Ophthalmic
Date received: 1987-04-10
Decision date: 1987-05-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Leandro, CA, US

Download summary PDF View on FDA.gov ↗

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