Thorek Scissors 7 1/4 & 10

FDA 510(k) K771806 · J. Sklar Mfg. Co., Inc.

Substantially Equivalent

510(k) numberK771806

Submission

Device name
Thorek Scissors 7 1/4 & 10
Applicant
J. Sklar Mfg. Co., Inc.
Mchenry, IL, US
Received
September 23, 1977
Decision date
October 4, 1977
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

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

Other 510(k)s with product code FZT

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K112400SmartshearsFZT · Traditional Nuscience Consulting and Management Group, LLC09/12/2011SE
K890818Auto Suture Disposable Surgical Trocar*FZT · Traditional United States Surgical, A Division of Tyco Healthc05/04/1989SE
K872990Micrins Surgical ScissorFZT · Traditional Micrins Surgical, Inc.08/17/1987SE
K841741Single Hair Transplant GraftFZT · Traditional Paris Products, Inc.07/23/1984SE
K841247SPC Disposable CutterFZT · Traditional Surgical Products Corp.05/02/1984SE
K822448Scissors, VariousFZT · Traditional J. Sklar Mfg. Co., Inc.09/14/1982SE
K821632Surgical Scissors, Set of 3FZT · Traditional Fred Sammons, Inc.06/24/1982SE
K821361Conphar Tonsil ScissorsFZT · Traditional Conphar, Inc.05/27/1982SE
K821355Conphar Littauer ScissorsFZT · Traditional Conphar, Inc.05/27/1982SE
K821352Conphar Iris ScissorsFZT · Traditional Conphar, Inc.05/27/1982SE

More from Conphar, Inc.

510(k)DeviceDecision
K843693Jacobs High Vacuum Suction Unit 05-2570BTA · Traditional 10/31/1984SE
K842112Tischler Cervical Biopsy Punch ForcepsHFB · Traditional 07/03/1984SE
K842111Kogan Endospeculum 9-1/2HTZ · Traditional 06/19/1984SE
K822448Scissors, VariousFZT · Traditional 09/14/1982SE
K802458Kevorkian-Younge Biopsy Curette #90-6611HFB · Traditional 01/12/1981SE
K802457Kevorkian-Younge Biopsy Punch, #90-6610HFB · Traditional 01/12/1981SE
K801273Magill Catheter Intro. ForcepsKOA · Traditional 07/28/1980SE
K800441Rudd-Clinic Hemorrhoidal ForcepsKOA · Traditional 04/08/1980SE
K790577Hemorrhoidal LigatorHCF · Traditional 04/23/1979SE
K772230Cannula, Perfusion, Fallopian TubeLKF · Traditional 01/03/1978SE

Questions and answers

When was Thorek Scissors 7 1/4 & 10 cleared by the FDA?

Thorek Scissors 7 1/4 & 10 (K771806) received a 510(k) decision of Substantially Equivalent on October 4, 1977, 11 days after the submission was received.

What is the product code of K771806?

The FDA product code is FZT – Cutter, Surgical, a Class I (low risk) device regulated under 21 CFR 878.4800.