Forceps

FDA 510(k) K904723 · Minto Research & Development, Inc.

Substantially Equivalent

510(k) numberK904723

Submission

Device name
Forceps
Applicant
Minto Research & Development, Inc.
Redding, CA, US
Received
October 17, 1990
Decision date
July 26, 1991
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
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
K891401Hemostatic Forceps Bruns.,Gemini,Spencer-Well,KantGEN · Traditional Zinnanti Surgical Instruments, Inc.04/06/1989SE

More from Zinnanti Surgical Instruments, Inc.

510(k)DeviceDecision
K940590Minto Skin Traction MotorITH · Traditional 04/15/1994SE
K904511Hand-Carried Stretchers/Break Away FlatFPP · Traditional 10/12/1990SE
K904494Hand-Carried StretchersFPP · Traditional 10/12/1990SE

Questions and answers

When was Forceps cleared by the FDA?

Forceps (K904723) received a 510(k) decision of Substantially Equivalent on July 26, 1991, 282 days after the submission was received.

What is the product code of K904723?

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