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FDA 510(k)

SCISSORS, WIRE CUTTING

K-Number: K884095 · 1988-10-19

ApplicantMagnatrade Corp.
Decision Date1988-10-19
Product CodeLRW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SCISSORS, WIRE CUTTING is the device name listed in this FDA 510(k) record. The listed applicant is Magnatrade Corp.. It received FDA 510(k) clearance on 1988-10-19 under 510(k) number K884095. The device is classified under product code LRW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCISSORS, WIRE CUTTING?

SCISSORS, WIRE CUTTING is a medical device that received FDA 510(k) clearance on 1988-10-19. The listed applicant is Magnatrade Corp.. The 510(k) number is K884095.

When did SCISSORS, WIRE CUTTING receive FDA 510(k) clearance?

SCISSORS, WIRE CUTTING received FDA 510(k) clearance on 1988-10-19, under 510(k) number K884095.

Who is the listed applicant for SCISSORS, WIRE CUTTING?

The FDA 510(k) record lists Magnatrade Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SCISSORS, WIRE CUTTING?

The FDA product code for SCISSORS, WIRE CUTTING is LRW.

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Related Devices (Code: LRW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K911158MICRO SCISSORS, 5MM CURVE MICRO SCISSORS, 5MMNorthgate Technologies, Inc.K902828SUTURE REMOVAL TRAYOrion Life Systems, Inc.K900957GS-2100 HOOK SUTURE SCISSOR, 5MMSolos Endoscopy, Inc.K900950GS-2000 MICRO SCISSOR, CURVED LEFT, 5MMSolos Endoscopy, Inc.K892823PLASTER CUTTING SCISSORSThe South India Surgical Co. Pvt. , Ltd.K891889OLIVECORONA SCISSORSZinnanti Surgical Instruments, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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