AESCULAP TROCAR INSTRUMENT SET— 510(k) K934724

Substantially Equivalent

Aesculap, Inc.

FDA 510(k) clearance K934724 for AESCULAP TROCAR INSTRUMENT SET, Substantially Equivalent on 1993-12-23. Applicant: Aesculap, Inc.. Device class: 2.

Clearance details

Applicant: Aesculap, Inc.
Product code: Code FBQ
Device class: Class 2
Regulation: 21 CFR 876.5090
Advisory panel: Gastroenterology, Urology
Date received: 1993-10-01
Decision date: 1993-12-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: South San Francisco, CA, 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.