Hartman Forceps Straight 3 1/2

FDA 510(k) K821278 · Conphar, Inc.

Substantially Equivalent

510(k) numberK821278

Submission

Device name
Hartman Forceps Straight 3 1/2
Applicant
Conphar, Inc.
Mchenry, IL, US
Received
May 3, 1982
Decision date
May 27, 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

More from Zinnanti Surgical Instruments, Inc.

510(k)DeviceDecision
K821825Conphar Silicone Feeding TubeKNT · Traditional 08/10/1982SE
K821354Conphar Mayo Hegar Needle HolderGDF · Traditional 06/03/1982SE
K821295Olsen Hegar Needle HoldersGDF · Traditional 06/03/1982SE
K821289Mayo-Hegar Needle HolderGDF · Traditional 06/03/1982SE
K821298Backhaus Clamp, 3 1/2HTD · Traditional 05/28/1982SE
K821294Tonsil Scissors Straight 5 1/2EGN · Traditional 05/28/1982SE
K821293Backhaus Clamp, 5 1/4HTD · Traditional 05/28/1982SE
K821292Tonsil Scissors 7EGN · Traditional 05/28/1982SE
K821290Littauer Scissors 5 1/2HNF · Traditional 05/28/1982SE
K821286Iris Scissors Straight 4 1/2HNF · Traditional 05/28/1982SE

Questions and answers

When was Hartman Forceps Straight 3 1/2 cleared by the FDA?

Hartman Forceps Straight 3 1/2 (K821278) received a 510(k) decision of Substantially Equivalent on May 27, 1982, 24 days after the submission was received.

What is the product code of K821278?

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