AXIOM TROCAR THORACIC CATHETER— 510(k) K863247

Name: FDA 510(k) clearance K863247
Creator: U.S. Food and Drug Administration
Published: 1986-08-29

Substantially Equivalent

Axiom Medical, Inc.

FDA 510(k) clearance K863247 for AXIOM TROCAR THORACIC CATHETER, Substantially Equivalent on 1986-08-29. 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: 1986-08-22
Decision date: 1986-08-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Paramount, CA, US

Download summary PDF View on FDA.gov ↗

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