VENTROFIL TENSION RELIEF SUTURE SET— 510(k) K904435

Name: FDA 510(k) clearance K904435
Creator: U.S. Food and Drug Administration
Published: 1991-08-29

Substantially Equivalent

Aesculap, Inc.

FDA 510(k) clearance K904435 for VENTROFIL TENSION RELIEF SUTURE SET, Substantially Equivalent on 1991-08-29. Applicant: Aesculap, Inc.. Device class: 1.

Clearance details

Applicant: Aesculap, Inc.
Product code: Code KGS
Device class: Class 1
Regulation: 21 CFR 878.4930
Advisory panel: General, Plastic Surgery
Date received: 1990-09-28
Decision date: 1991-08-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Burlingame, 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.