Scissors, Wire Cutting

FDA 510(k) K884095 · Magnatrade Corp.

Substantially Equivalent

510(k) numberK884095

Submission

Device name
Scissors, Wire Cutting
Applicant
Magnatrade Corp.
Tulsa, OK, US
Received
September 28, 1988
Decision date
October 19, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
LRW – Scissors, General, Surgical
Device class
Class I (low risk)
Regulation
21 CFR 878.4800
Specialty
General, Plastic Surgery

Other 510(k)s with product code LRW

510(k)DeviceApplicantDecision
K911158Micro Scissors, 5MM Curve Micro Scissors, 5MMLRW · Traditional Northgate Technologies, Inc.03/29/1991SE
K902828Suture Removal TrayLRW · Traditional Orion Life Systems, Inc.08/08/1990SEKD
K900957GS-2100 Hook Suture Scissor, 5MMLRW · Traditional Solos Endoscopy, Inc.04/18/1990SE
K900950GS-2000 Micro Scissor, Curved Left, 5MMLRW · Traditional Solos Endoscopy, Inc.04/18/1990SE
K892823Plaster Cutting ScissorsLRW · Traditional The South India Surgical Co. Pvt. , Ltd.05/25/1989SE
K891889Olivecorona ScissorsLRW · Traditional Zinnanti Surgical Instruments, Inc.04/12/1989SE
K891886Scissors, Various TypesLRW · Traditional Zinnanti Surgical Instruments, Inc.04/12/1989SE
K891203Scissors: Thorek, Jorgensen, FinochiettoLRW · Traditional Zinnanti Surgical Instruments, Inc.04/06/1989SE
K891200Ribbon Type Scissors: Tenotomy,Iris,Eye,StrabismusLRW · Traditional Zinnanti Surgical Instruments, Inc.04/06/1989SE
K890235Dressing ScissorsLRW · Traditional Kinetic Medical Products02/03/1989SE

Questions and answers

When was Scissors, Wire Cutting cleared by the FDA?

Scissors, Wire Cutting (K884095) received a 510(k) decision of Substantially Equivalent on October 19, 1988, 21 days after the submission was received.

What is the product code of K884095?

The FDA product code is LRW – Scissors, General, Surgical, a Class I (low risk) device regulated under 21 CFR 878.4800.