Modified Auto Suture Purstring Disp. Automatic

FDA 510(k) K901107 · United States Surgical, A Division of Tyco Healthc

Substantially Equivalent

510(k) numberK901107

Submission

Device name
Modified Auto Suture Purstring Disp. Automatic
Applicant
United States Surgical, A Division of Tyco Healthc
Norwalk, CT, US
Received
March 8, 1990
Decision date
April 9, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

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

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More from Stuart-Lee, Inc.

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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 Modified Auto Suture Purstring Disp. Automatic cleared by the FDA?

Modified Auto Suture Purstring Disp. Automatic (K901107) received a 510(k) decision of Substantially Equivalent on April 9, 1990, 32 days after the submission was received.

What is the product code of K901107?

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