GIMMI ANEURYSM CLIPS AND APPLYING FORCEPS— 510(k) K081640

Name: FDA 510(k) clearance K081640
Creator: U.S. Food and Drug Administration
Published: 2009-05-06

Substantially Equivalent

Gimmi GmbH

FDA 510(k) clearance K081640 for GIMMI ANEURYSM CLIPS AND APPLYING FORCEPS, Substantially Equivalent on 2009-05-06. Applicant: Gimmi GmbH. Device class: 2.

Clearance details

Applicant: Gimmi GmbH
Product code: Code HCH
Device class: Class 2
Regulation: 21 CFR 882.5200
Advisory panel: Neurology
Date received: 2008-06-11
Decision date: 2009-05-06
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Saint Paul, MN, US

Download summary PDF View on FDA.gov ↗

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