OPHTHALMOSCOPE, BINOCULAR, INDIRECT— 510(k) K772214

Name: FDA 510(k) clearance K772214
Creator: U.S. Food and Drug Administration
Published: 1977-12-13

Substantially Equivalent

Varian Assoc., Inc.

FDA 510(k) clearance K772214 for OPHTHALMOSCOPE, BINOCULAR, INDIRECT, Substantially Equivalent on 1977-12-13. Applicant: Varian Assoc., Inc.. Device class: 2.

Clearance details

Applicant: Varian Assoc., Inc.
Product code: Code HLI
Device class: Class 2
Regulation: 21 CFR 886.1570
Advisory panel: Ophthalmic
Date received: 1977-12-02
Decision date: 1977-12-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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