AESCULAP TROCAR INSTRUMENT SET— 510(k) K933201

Substantially Equivalent

Aesculap, Inc.

FDA 510(k) clearance K933201 for AESCULAP TROCAR INSTRUMENT SET, Substantially Equivalent on 1993-09-13. Applicant: Aesculap, Inc.. Device class: 2.

Clearance details

Applicant: Aesculap, Inc.
Product code: Code GCS
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 1993-07-01
Decision date: 1993-09-13
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.