Endoscope

FDA 510(k) K944555 · United States Surgical, A Division of Tyco Healthc

Substantially Equivalent

510(k) numberK944555

Submission

Device name
Endoscope
Applicant
United States Surgical, A Division of Tyco Healthc
Norwalk, CT, US
Received
September 16, 1994
Decision date
December 30, 1994
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HET – Laparoscope, Gynecologic (And Accessories)
Device class
Class II (moderate risk)
Regulation
21 CFR 884.1720
Specialty
Obstetrics/Gynecology

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More from 270surgical , Ltd.

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K061288Auto Suture Endo Clip III 5 MM Clip ApplierFZP · Special 11/02/2006SE
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 Endoscope cleared by the FDA?

Endoscope (K944555) received a 510(k) decision of Substantially Equivalent on December 30, 1994, 105 days after the submission was received.

What is the product code of K944555?

The FDA product code is HET – Laparoscope, Gynecologic (And Accessories), a Class II (moderate risk) device regulated under 21 CFR 884.1720.