Adt Disposable Scalpel W/Stainless Steel

FDA 510(k) K830745 · Lab Industries, Inc.

Substantially Equivalent

510(k) numberK830745

Submission

Device name
Adt Disposable Scalpel W/Stainless Steel
Applicant
Lab Industries, Inc.
Mchenry, IL, US
Received
March 8, 1983
Decision date
April 12, 1983
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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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.

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Questions and answers

When was Adt Disposable Scalpel W/Stainless Steel cleared by the FDA?

Adt Disposable Scalpel W/Stainless Steel (K830745) received a 510(k) decision of Substantially Equivalent on April 12, 1983, 35 days after the submission was received.

What is the product code of K830745?

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