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FDA 510(k)

SCISSORS

K-Number: K890170 · 1989-02-03

ApplicantDhason Brothers, Inc.
Decision Date1989-02-03
Product CodeLRW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SCISSORS is the device name listed in this FDA 510(k) record. The listed applicant is Dhason Brothers, Inc.. It received FDA 510(k) clearance on 1989-02-03 under 510(k) number K890170. 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?

SCISSORS is a medical device that received FDA 510(k) clearance on 1989-02-03. The listed applicant is Dhason Brothers, Inc.. The 510(k) number is K890170.

When did SCISSORS receive FDA 510(k) clearance?

SCISSORS received FDA 510(k) clearance on 1989-02-03, under 510(k) number K890170.

Who is the listed applicant for SCISSORS?

The FDA 510(k) record lists Dhason Brothers, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SCISSORS?

The FDA product code for SCISSORS is LRW.

Related Clinical Trials

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.

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Other records listing Dhason Brothers, Inc. as applicant

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.

K890156IMPACTOR FOR FEMORAL HEADK890162EXTRACTOR FOR AUSTIN MOORE FEMORAL HEADK890165FORCEPS-ORTHOPEDICK890164HUDSON BRACE W/BURRSK890168RETRACTOR, SELF-RETAININGK890161THOMPSON TYPE RASP W/TOMMY BAR

View all 14 devices →

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.K900950GS-2000 MICRO SCISSOR, CURVED LEFT, 5MMSolos Endoscopy, Inc.K900957GS-2100 HOOK SUTURE SCISSOR, 5MMSolos Endoscopy, Inc.K892823PLASTER CUTTING SCISSORSThe South India Surgical Co. Pvt. , Ltd.K891889OLIVECORONA SCISSORSZinnanti Surgical Instruments, Inc.

Official Source

View on FDA Database →

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

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