VISTA FINOFF TRANSILLUMINATOR (AC-POWERED)— 510(k) K893170

Name: FDA 510(k) clearance K893170
Creator: U.S. Food and Drug Administration
Published: 1989-06-05

Substantially Equivalent

Keeler Instruments, Inc.

FDA 510(k) clearance K893170 for VISTA FINOFF TRANSILLUMINATOR (AC-POWERED), Substantially Equivalent on 1989-06-05. Applicant: Keeler Instruments, Inc.. Device class: 2.

Clearance details

Applicant: Keeler Instruments, Inc.
Product code: Code HJM
Device class: Class 2
Regulation: 21 CFR 886.1945
Advisory panel: Ophthalmic
Date received: 1989-04-25
Decision date: 1989-06-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Broomall, PA, US

Download summary PDF View on FDA.gov ↗

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