AESCULAP PNEUMATIC KERRISON— 510(k) K062413

Substantially Equivalent

Aesculap, Inc.

FDA 510(k) clearance K062413 for AESCULAP PNEUMATIC KERRISON, Substantially Equivalent on 2006-11-21. Applicant: Aesculap, Inc..

Clearance details

Applicant: Aesculap, Inc.
Product code: Code HAD
Advisory panel: Neurology
Date received: 2006-08-17
Decision date: 2006-11-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Center Valley, PA, US

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