DURALASTIC SILICONE TUBING— 510(k) K955433

Name: FDA 510(k) clearance K955433
Creator: U.S. Food and Drug Administration
Published: 1996-01-26

Substantially Equivalent

Allied Biomedical Corp.

FDA 510(k) clearance K955433 for DURALASTIC SILICONE TUBING, Substantially Equivalent on 1996-01-26. Applicant: Allied Biomedical Corp.. Device class: 1.

Clearance details

Applicant: Allied Biomedical Corp.
Product code: Code KGZ
Device class: Class 1
Regulation: 21 CFR 878.4200
Advisory panel: General, Plastic Surgery
Date received: 1995-11-28
Decision date: 1996-01-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Paso Robles, CA, US

Download summary PDF View on FDA.gov ↗

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