Retrieval Forceps W/Alligator Jaws

FDA 510(k) K820968 · Mill-Rose Laboratory

Substantially Equivalent

510(k) numberK820968

Submission

Device name
Retrieval Forceps W/Alligator Jaws
Applicant
Mill-Rose Laboratory
Mchenry, IL, US
Received
April 6, 1982
Decision date
April 26, 1982
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

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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

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K971275Mill-Rose Disposable Polypectomy SnareFDI · Traditional 05/23/1997SE
K962736Mill-Rose Laryngoscopic Injection NeedleEOQ · Traditional 07/29/1996SE
K960880Mill-Rose Blind Microbiology BrushEOQ · Traditional 04/29/1996SE
K954519Wang Transendoscopic Aspiration NeedleFBK · Traditional 12/22/1995SE
K951600Mill-Rose Rotatable Polypectomy SnareFDI · Traditional 12/18/1995SE
K954745Mill-Rose Rigid Scope Cleaning BrushesFEB · Traditional 11/27/1995SE
K951051Rite-Bite Biopsy ForcepsEOQ · Traditional 03/24/1995SE
K951048Rite-Bite Biopsy ForcepsFCL · Traditional 03/15/1995SE

Questions and answers

When was Retrieval Forceps W/Alligator Jaws cleared by the FDA?

Retrieval Forceps W/Alligator Jaws (K820968) received a 510(k) decision of Substantially Equivalent on April 26, 1982, 20 days after the submission was received.

What is the product code of K820968?

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