Dispos. & Sponge Forceps Pean Artery

FDA 510(k) K843074 · Greene International Corp.

Substantially Equivalent

510(k) numberK843074

Submission

Device name
Dispos. & Sponge Forceps Pean Artery
Applicant
Greene International Corp.
Mchenry, IL, US
Received
August 6, 1984
Decision date
August 17, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
GEN – Forceps, General & Plastic Surgery
Device class
Class I (low risk)
Regulation
21 CFR 878.4800
Specialty
General, Plastic Surgery

Other 510(k)s with product code GEN

510(k)DeviceApplicantDecision
K031828Naturalase LP Nd:Yag LaserGEN · Traditional Focus Medical, LLC07/17/2003SE
K953962ForcepsGEN · Traditional Biopsys Medical, Inc.09/08/1995SE
K932385Suture Removing ForcepsGEN · Traditional Rocket of London, Ltd.08/06/1993SE
K904723ForcepsGEN · Traditional Minto Research & Development, Inc.07/26/1991SE
K911159Palpation ProbeGEN · Traditional Northgate Technologies, Inc.03/29/1991SE
K900960GS-1500 Claw Forcep, 10MMGEN · Traditional Solos Endoscopy, Inc.04/18/1990SE
K900952GS-1200 Grasping/Extracting Forcep, 10MMGEN · Traditional Solos Endoscopy, Inc.04/18/1990SE
K900951GS-7000 Clip-Applying Forcep, 10MM, Medium ClipGEN · Traditional Solos Endoscopy, Inc.04/18/1990SE
K900948GS-1002 Grasping Forcep, 5MM with RatchetGEN · Traditional Solos Endoscopy, Inc.04/18/1990SE
K891896Tissue Forceps, Various TypesGEN · Traditional Zinnanti Surgical Instruments, Inc.04/12/1989SE

More from Zinnanti Surgical Instruments, Inc.

510(k)DeviceDecision
K883827Masks, Various Types of Surgical MasksFXX · Traditional 11/17/1988SE
K883828Cone Masks, Various Types of Surgical Cone MasksFXX · Traditional 10/03/1988SE
K880484Surgical GarmentsFYC · Traditional 06/27/1988SE
K870617Various Tyes of Surgical GarmentsFYF · Traditional 03/09/1987SE
K843075Utility Scissors Disposable ItemsJOK · Traditional 09/05/1984SE
K843073Fixed Vol. Dispensers, Adjust Vol-HunpipJQW · Traditional 08/24/1984SE
K842719Standard WheelchairIQC · Traditional 07/25/1984SE

Questions and answers

When was Dispos. & Sponge Forceps Pean Artery cleared by the FDA?

Dispos. & Sponge Forceps Pean Artery (K843074) received a 510(k) decision of Substantially Equivalent on August 17, 1984, 11 days after the submission was received.

What is the product code of K843074?

The FDA product code is GEN – Forceps, General & Plastic Surgery, a Class I (low risk) device regulated under 21 CFR 878.4800.