Disposable #11 Scalpel Blade W/Short

FDA 510(k) K820869 · Van-Tec, Inc.

Substantially Equivalent

510(k) numberK820869

Submission

Device name
Disposable #11 Scalpel Blade W/Short
Applicant
Van-Tec, Inc.
Walker, MI, US
Received
March 29, 1982
Decision date
May 5, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
GDX – Scalpel, One-Piece
Device class
Class I (low risk)
Regulation
21 CFR 878.4800
Specialty
General, Plastic Surgery

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K904505Cci Corneal ScarifierGDX · Traditional Buckman Co., Inc.04/23/1991SE
K9053801-CUT Acl Graft KnifeGDX · Traditional Depuy, Inc.12/13/1990SE
K895682Vessel LoopsGDX · Traditional Applied Medical Technologies10/24/1989SE
K893033Mini-Diamond KnifeGDX · Traditional L.A.B. Instruments05/26/1989SE
K880028Omed Disposable ScalpelGDX · Traditional Oxboro Medical Intl., Inc.01/29/1988SE
K871894KCK Industries' Surgical InstrumentsGDX · Traditional Kck Industries06/23/1987SE
K863950P.S.I.-Disposable Metal Handle Surgeons ScalpelGDX · Traditional Precision Surgical Industries, Inc.10/24/1986SE

More from Precision Surgical Industries, Inc.

510(k)DeviceDecision
K880099Van-Tec Bladder EvacuatorKQT · Traditional 03/02/1988SE
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K880096Van-Tec Aspiration Biopsy System W/Collection CupKNW · Traditional 03/02/1988SE
K880095Berger Prostate Culture Cytology BrushFDX · Traditional 03/02/1988SE
K880094Van-Tec Endopyelotomy KnifeEMF · Traditional 02/29/1988SE
K874112Van-Tec Double Occlusion Balloon CatheterKOD · Traditional 02/11/1988SE
K871779Helical Stone Basket (Disposable)FFL · Traditional 06/17/1987SE
K871777Van-Tec Reusable Helical Stone BasketFFL · Traditional 06/17/1987SE
K870696Van-Tec Segura Stone Basket W/Protective SheathFFL · Traditional 03/30/1987SE
K870679Van-Tec Modular Flexible CystourethroscopeFBO · Traditional 03/30/1987SE

Questions and answers

When was Disposable #11 Scalpel Blade W/Short cleared by the FDA?

Disposable #11 Scalpel Blade W/Short (K820869) received a 510(k) decision of Substantially Equivalent on May 5, 1982, 37 days after the submission was received.

What is the product code of K820869?

The FDA product code is GDX – Scalpel, One-Piece, a Class I (low risk) device regulated under 21 CFR 878.4800.