AESCULAP AXIAL CLIP APPLIER— 510(k) K984109

Substantially Equivalent

Aesculap, Inc.

FDA 510(k) clearance K984109 for AESCULAP AXIAL CLIP APPLIER, Substantially Equivalent on 1999-02-12. Applicant: Aesculap, Inc..

Clearance details

Applicant: Aesculap, Inc.
Product code: Code HCI
Advisory panel: Neurology
Date received: 1998-11-17
Decision date: 1999-02-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: South San Francisco, CA, US

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