Pilling Diamond Knife

FDA 510(k) K822749 · Narco Scientific

Substantially Equivalent

510(k) numberK822749

Submission

Device name
Pilling Diamond Knife
Applicant
Narco Scientific
Mchenry, IL, US
Received
September 10, 1982
Decision date
October 6, 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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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
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Questions and answers

When was Pilling Diamond Knife cleared by the FDA?

Pilling Diamond Knife (K822749) received a 510(k) decision of Substantially Equivalent on October 6, 1982, 26 days after the submission was received.

What is the product code of K822749?

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