PAJUNK'S PRIMOCUT DISPOSABLE BIOPSY SYSTEM— 510(k) K080674

Name: FDA 510(k) clearance K080674
Creator: U.S. Food and Drug Administration
Published: 2008-05-09

Substantially Equivalent

PAJUNK GmbH Medizintechnologie

FDA 510(k) clearance K080674 for PAJUNK'S PRIMOCUT DISPOSABLE BIOPSY SYSTEM, Substantially Equivalent on 2008-05-09. Applicant: PAJUNK GmbH Medizintechnologie. Device class: 1.

Clearance details

Applicant: PAJUNK GmbH Medizintechnologie
Product code: Code MJG
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 2008-03-10
Decision date: 2008-05-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Geisingen, DE

Download summary PDF View on FDA.gov ↗

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