THE KIRSCHNER UNIVERSAL POWER TOOL SYSTEM— 510(k) K901455

Name: FDA 510(k) clearance K901455
Creator: U.S. Food and Drug Administration
Published: 1990-05-14

Substantially Equivalent

Kirschner Medical Corp.

FDA 510(k) clearance K901455 for THE KIRSCHNER UNIVERSAL POWER TOOL SYSTEM, Substantially Equivalent on 1990-05-14. Applicant: Kirschner Medical Corp.. Device class: 1.

Clearance details

Applicant: Kirschner Medical Corp.
Product code: Code HSZ
Device class: Class 1
Regulation: 21 CFR 878.4820
Advisory panel: General, Plastic Surgery
Date received: 1990-04-02
Decision date: 1990-05-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Timonium, MD, US

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