Micrins Forceps 2010

FDA 510(k) K872991 · Micrins Surgical, Inc.

Substantially Equivalent

510(k) numberK872991

Submission

Device name
Micrins Forceps 2010
Applicant
Micrins Surgical, Inc.
Chicago, IL, US
Received
July 31, 1987
Decision date
August 17, 1987
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
K993970Micrins Microsurgical SutureGAR · Traditional 03/30/2000SE
K982278Micrins Micro Anastomosis ClampDXC · Traditional 03/26/1999SE
K933310Micrins Contrast Background MaterialEPT · Traditional 08/19/1993SE
K872989Micrins Needle HolderHXK · Traditional 08/21/1987SE
K872990Micrins Surgical ScissorFZT · Traditional 08/17/1987SE

Questions and answers

When was Micrins Forceps 2010 cleared by the FDA?

Micrins Forceps 2010 (K872991) received a 510(k) decision of Substantially Equivalent on August 17, 1987, 17 days after the submission was received.

What is the product code of K872991?

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