CLINICAL WIDEFIELD SPECULAR MICRISCOPE 500— 510(k) K852150

Name: FDA 510(k) clearance K852150
Creator: U.S. Food and Drug Administration
Published: 1985-06-03

Substantially Equivalent

Keeler Instruments, Inc.

FDA 510(k) clearance K852150 for CLINICAL WIDEFIELD SPECULAR MICRISCOPE 500, Substantially Equivalent on 1985-06-03. Applicant: Keeler Instruments, Inc.. Device class: 1.

Clearance details

Applicant: Keeler Instruments, Inc.
Product code: Code HRM
Device class: Class 1
Regulation: 21 CFR 878.4700
Advisory panel: General, Plastic Surgery
Date received: 1985-05-17
Decision date: 1985-06-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Broomall, PA, US

Download summary PDF View on FDA.gov ↗

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