AESCULAP'S MODULAR ENDOSCOPIC INSTRUMENTS FOR GYNECOLOGY— 510(k) K010752

Substantially Equivalent

Aesculap, Inc.

FDA 510(k) clearance K010752 for AESCULAP'S MODULAR ENDOSCOPIC INSTRUMENTS FOR GYNECOLOGY, Substantially Equivalent on 2001-06-11. Applicant: Aesculap, Inc..

Clearance details

Applicant: Aesculap, Inc.
Product code: Code KNF
Advisory panel: Obstetrics/Gynecology
Date received: 2001-03-13
Decision date: 2001-06-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Center Valley, PA, US

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