AESULAP KOPITNIK AVM MICROCLIPS AND APPLIER— 510(k) K024349

Name: FDA 510(k) clearance K024349
Creator: U.S. Food and Drug Administration
Published: 2003-03-24

Substantially Equivalent

Aesculap, Inc.

FDA 510(k) clearance K024349 for AESULAP KOPITNIK AVM MICROCLIPS AND APPLIER, Substantially Equivalent on 2003-03-24. Applicant: Aesculap, Inc.. Device class: 2.

Clearance details

Applicant: Aesculap, Inc.
Product code: Code HCH
Device class: Class 2
Regulation: 21 CFR 882.5200
Advisory panel: Neurology
Date received: 2002-12-30
Decision date: 2003-03-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Center Valley, PA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.