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FDA 510(k)

AART SILICONE TUBING

K-Number: K022306 · 2002-10-10

ApplicantAesthetic and Reconstructive Technologies, Inc.
Decision Date2002-10-10
Product CodeKGZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AART SILICONE TUBING is the device name listed in this FDA 510(k) record. The listed applicant is Aesthetic and Reconstructive Technologies, Inc.. It received FDA 510(k) clearance on 2002-10-10 under 510(k) number K022306. The device is classified under product code KGZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AART SILICONE TUBING?

AART SILICONE TUBING is a medical device that received FDA 510(k) clearance on 2002-10-10. The listed applicant is Aesthetic and Reconstructive Technologies, Inc.. The 510(k) number is K022306.

When did AART SILICONE TUBING receive FDA 510(k) clearance?

AART SILICONE TUBING received FDA 510(k) clearance on 2002-10-10, under 510(k) number K022306.

Who is the listed applicant for AART SILICONE TUBING?

The FDA 510(k) record lists Aesthetic and Reconstructive Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AART SILICONE TUBING?

The FDA product code for AART SILICONE TUBING is KGZ.

Related Clinical Trials

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Other records listing Aesthetic and Reconstructive Technologies, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K023678DIMISIL SCAR GELK022511AART CALF IMPLANTK022223AART SILICONE SHEETINGK021820AART SILICONE CARVING BLOCKK021839AART GLUTEAL IMPLANTK021337AART PECTORALIS IMPLANT

View all 10 devices →

Related Devices (Code: KGZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K974295BYRON MEDICAL ASPIRATION AND INFILTRATION/IRRIGATION TUBINGByron MedicalK973183WOUND DRAINAGE HOLDERR & D Medical Products, Inc.K955433DURALASTIC SILICONE TUBINGAllied Biomedical Corp.K942315NAVARRE PERCUTANEOUS ACCESS SETNavarre Biomedical , Ltd.K896087PALESTRANT IRRIGATION AND DRAINAGE SETNorth American Instrument Corp.K895041OPTICAL CATHETER(TM) INTRODUCER SETSMedical Dynamics, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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