VICKERS ERGOMATIC MICROSUR INSTRU-UNIV R O L HAND— 510(k) K853179

Name: FDA 510(k) clearance K853179
Creator: U.S. Food and Drug Administration
Published: 1985-11-07

Substantially Equivalent

Keeler Instruments, Inc.

FDA 510(k) clearance K853179 for VICKERS ERGOMATIC MICROSUR INSTRU-UNIV R O L HAND, Substantially Equivalent on 1985-11-07. Applicant: Keeler Instruments, Inc.. Device class: 1.

Clearance details

Applicant: Keeler Instruments, Inc.
Product code: Code GZX
Device class: Class 1
Regulation: 21 CFR 882.4525
Advisory panel: Neurology
Date received: 1985-07-30
Decision date: 1985-11-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Broomall, PA, US

Download summary PDF View on FDA.gov ↗

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