Scalpel, One-Piece, Disposable

FDA 510(k) K854857 · Medelec Intl. Corp.

Substantially Equivalent

510(k) numberK854857

Submission

Device name
Scalpel, One-Piece, Disposable
Applicant
Medelec Intl. Corp.
Miami Beach, FL, US
Received
December 5, 1985
Decision date
December 24, 1985
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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K914086Ican Cylindrical SpongesGDX · Traditional Icn Pharmaceuticals, Inc.10/09/1991SE
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
K961013Disposable Needle ElectrodeIKT · Traditional 12/20/1996SE
K935017TD50 ElectromyographJXE · Traditional 07/28/1994SE
K922548Medelec 2110 and 2114 EEGGWQ · Traditional 11/03/1992SE
K920127Electroencephalograph Recording SystemGWQ · Traditional 06/10/1992SE
K912775Sapphire 4ME Emg/Ep SystemGWF · Traditional 11/08/1991SE
K865106Prophylactic (Condom) Mr. JohnnyHIS · Traditional 05/20/1987SE
K863491Blood Specimen Collection DevicesJKA · Traditional 10/24/1986SE
K854622Prophylactic (Condom)HIS · Traditional 04/11/1986SE
K854562Connector, Blood Tubing, Infusion T. Intravenous IBRZ · Traditional 01/09/1986SE
K854860Blades, Scalpel Carbon SteetGES · Traditional 12/24/1985SE

Questions and answers

When was Scalpel, One-Piece, Disposable cleared by the FDA?

Scalpel, One-Piece, Disposable (K854857) received a 510(k) decision of Substantially Equivalent on December 24, 1985, 19 days after the submission was received.

What is the product code of K854857?

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