Auto Suture Surgiport Cannula Diameter Reducer*

FDA 510(k) K896434 · United States Surgical, A Division of Tyco Healthc

Substantially Equivalent

510(k) numberK896434

Submission

Device name
Auto Suture Surgiport Cannula Diameter Reducer*
Applicant
United States Surgical, A Division of Tyco Healthc
Norwalk, CT, US
Received
November 9, 1989
Decision date
November 16, 1989
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
GEA – Cannula, Surgical, General & Plastic Surgery
Device class
Class I (low risk)
Regulation
21 CFR 878.4800
Specialty
General, Plastic Surgery

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K954599Conmed Trogard Electronic Trocar SystemGEA · Traditional Conmedcorp11/27/1995SE
K922460Origin Secondary Cannula and TrocarGEA · Traditional Origin Medsystems, Inc.09/16/1992SE
K920110Endopath Disposable Thoracic Trocar SleeveGEA · Traditional ETHICON, Inc.04/02/1992SE
K911262Disposable Specimen Bag W/Cannula and IntroducerGEA · Traditional ETHICON, Inc.06/20/1991SE
K904881Disposable Yankauer Suction TubeGEA · Traditional Pilling Medical S.A.03/06/1991SE
K903416Cannula, SurgicalGEA · Traditional Advantage Diagnostics Corp.11/23/1990SE
K904218Suction SystemGEA · Traditional Axiom Medical, Inc.10/31/1990SE
K901718Klein Lamprey-Cannula(Tm)GEA · Traditional Jeff Klein Surgical, Inc.05/24/1990SE

More from Jeff Klein Surgical, Inc.

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K062850Autosuture Circular Eea Surgical StaplersGDW · Special 10/23/2006SE
K062326Autosuture Modified Versaport Trocar with Fixation SleeveGCJ · Special 09/01/2006SE
K061095Auto Sutur Endo Gia StaplersGDW · Traditional 05/31/2006SE
K050947Modification to: Modified Uss Polypropylene SutureGAW · Special 06/01/2005SE
K042412Modified Spacemaker SystemGCJ · Special 09/24/2004SE
K040594Herculon Soft Tissue Reattachment SystemHWC · Special 03/31/2004SE
K032696Auto Suture Endoscopic (& Open) Ta Surgical Stapler, Auto Suture Endoscopic (& Open) Gia…GDW · Traditional 12/01/2003SE

Questions and answers

When was Auto Suture Surgiport Cannula Diameter Reducer* cleared by the FDA?

Auto Suture Surgiport Cannula Diameter Reducer* (K896434) received a 510(k) decision of Substantially Equivalent on November 16, 1989, 7 days after the submission was received.

What is the product code of K896434?

The FDA product code is GEA – Cannula, Surgical, General & Plastic Surgery, a Class I (low risk) device regulated under 21 CFR 878.4800.