AESCULAP YASARGIL ANEURYSM CLIP PHYNOX BOOSTER CLIP— 510(k) K032198

Name: FDA 510(k) clearance K032198
Creator: U.S. Food and Drug Administration
Published: 2003-08-20

Substantially Equivalent

Aesculap, Inc.

FDA 510(k) clearance K032198 for AESCULAP YASARGIL ANEURYSM CLIP PHYNOX BOOSTER CLIP, Substantially Equivalent on 2003-08-20. 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: 2003-07-18
Decision date: 2003-08-20
Decision: Substantially Equivalent
Clearance type: Special
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.