AXIOM ATRAUM TROCAR CATHETER— 510(k) K852241

Name: FDA 510(k) clearance K852241
Creator: U.S. Food and Drug Administration
Published: 1985-06-14

Substantially Equivalent

Axiom Medical, Inc.

FDA 510(k) clearance K852241 for AXIOM ATRAUM TROCAR CATHETER, Substantially Equivalent on 1985-06-14. Applicant: Axiom Medical, Inc.. Device class: 1.

Clearance details

Applicant: Axiom Medical, Inc.
Product code: Code GBS
Device class: Class 1
Regulation: 21 CFR 878.4200
Advisory panel: General, Plastic Surgery
Date received: 1985-05-23
Decision date: 1985-06-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Paramount, CA, US

Download summary PDF View on FDA.gov ↗

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