GS-1500 Claw Forcep, 10MM

FDA 510(k) K900960 · Solos Endoscopy, Inc.

Substantially Equivalent

510(k) numberK900960

Submission

Device name
GS-1500 Claw Forcep, 10MM
Applicant
Solos Endoscopy, Inc.
Norcross, GA, US
Received
February 27, 1990
Decision date
April 18, 1990
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
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
K891401Hemostatic Forceps Bruns.,Gemini,Spencer-Well,KantGEN · Traditional Zinnanti Surgical Instruments, Inc.04/06/1989SE

More from Zinnanti Surgical Instruments, Inc.

510(k)DeviceDecision
K983538Miniaturized Biopsy,Scope A.K.A: Biopsy Needle with Endoscopic Viewing CapabilityGCJ · Special 11/06/1998SE
K910671Model GS-4700 Common Duct Stone Removing KitFGE · Traditional 05/10/1991SE
K900965GS-4550 Trocar Only, 11MMFBM · Traditional 04/18/1990SE
K900964Cannula and Trocar, 11MMFBM · Traditional 04/18/1990SE
K900963GS-4350 Trocar Only, 5.5MMFBM · Traditional 04/18/1990SE
K900962GS-4300 Cannula and Trocar, 5.5MMFBM · Traditional 04/18/1990SE
K900961GS-4100 Reducer Sleeve, 5MM to 3MMFBM · Traditional 04/18/1990SE
K900959GS-1400 Toothed Dissecting Forcep, 5MM, InsulatedGEJ · Traditional 04/18/1990SE
K900958GS-1300 Atraumatic Grasping Forcep, Curved, 10MMGEJ · Traditional 04/18/1990SE
K900957GS-2100 Hook Suture Scissor, 5MMLRW · Traditional 04/18/1990SE

Questions and answers

When was GS-1500 Claw Forcep, 10MM cleared by the FDA?

GS-1500 Claw Forcep, 10MM (K900960) received a 510(k) decision of Substantially Equivalent on April 18, 1990, 50 days after the submission was received.

What is the product code of K900960?

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