POMERANTZEFF EQUATOR PLUS CAMERA— 510(k) K770888

Name: FDA 510(k) clearance K770888
Creator: U.S. Food and Drug Administration
Published: 1977-06-03

Substantially Equivalent

Medical Instrument Research Assoc., Inc.

FDA 510(k) clearance K770888 for POMERANTZEFF EQUATOR PLUS CAMERA, Substantially Equivalent on 1977-06-03. Applicant: Medical Instrument Research Assoc., Inc.. Device class: 2.

Clearance details

Applicant: Medical Instrument Research Assoc., Inc.
Product code: Code HKI
Device class: Class 2
Regulation: 21 CFR 886.1120
Advisory panel: Ophthalmic
Date received: 1977-05-16
Decision date: 1977-06-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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