AART SILICONE TUBING— 510(k) K022306

Name: FDA 510(k) clearance K022306
Creator: U.S. Food and Drug Administration
Published: 2002-10-10

Substantially Equivalent

Aesthetic and Reconstructive Technologies, Inc.

FDA 510(k) clearance K022306 for AART SILICONE TUBING, Substantially Equivalent on 2002-10-10. Applicant: Aesthetic and Reconstructive Technologies, Inc.. Device class: 1.

Clearance details

Applicant: Aesthetic and Reconstructive Technologies, Inc.
Product code: Code KGZ
Device class: Class 1
Regulation: 21 CFR 878.4200
Advisory panel: General, Plastic Surgery
Date received: 2002-07-16
Decision date: 2002-10-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Paso Robles, CA, US

Download summary PDF View on FDA.gov ↗

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K942315 — NAVARRE PERCUTANEOUS ACCESS SET1994-07-08
K896087 — PALESTRANT IRRIGATION AND DRAINAGE SET1989-11-03

More clearances from Aesthetic and Reconstructive Technologies, Inc.

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K023678 — DIMISIL SCAR GEL2003-01-23
K022511 — AART CALF IMPLANT2002-08-26
K022223 — AART SILICONE SHEETING2002-08-08
K021820 — AART SILICONE CARVING BLOCK2002-07-16
K021839 — AART GLUTEAL IMPLANT2002-07-16

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