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FDA 510(k)

DISPOSABLE SURGICAL SCISSORS AND FORCEPS

K-Number: K943229 · 1994-08-19

ApplicantY.M.K. International Co., Ltd.
Decision Date1994-08-19
Product CodeKDC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE SURGICAL SCISSORS AND FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Y.M.K. International Co., Ltd.. It received FDA 510(k) clearance on 1994-08-19 under 510(k) number K943229. The device is classified under product code KDC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE SURGICAL SCISSORS AND FORCEPS?

DISPOSABLE SURGICAL SCISSORS AND FORCEPS is a medical device that received FDA 510(k) clearance on 1994-08-19. The listed applicant is Y.M.K. International Co., Ltd.. The 510(k) number is K943229.

When did DISPOSABLE SURGICAL SCISSORS AND FORCEPS receive FDA 510(k) clearance?

DISPOSABLE SURGICAL SCISSORS AND FORCEPS received FDA 510(k) clearance on 1994-08-19, under 510(k) number K943229.

Who is the listed applicant for DISPOSABLE SURGICAL SCISSORS AND FORCEPS?

The FDA 510(k) record lists Y.M.K. International Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISPOSABLE SURGICAL SCISSORS AND FORCEPS?

The FDA product code for DISPOSABLE SURGICAL SCISSORS AND FORCEPS is KDC.

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Related Devices (Code: KDC)

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.

K936226SURGIMED BREAST LOCALIZATION NEEDLE WIRE SETMeadox Medicals, Div. Boston Scientific Corp.K920153THERMUFF BAGTechstylesK920263MANUAL SURGICAL INSTRUMENTSPhoenix Instruments Div.K915064DISPOSABLE CAUTERY ABRASIVE PADAmerican Medical Mfg., Inc.K914960INSTRUMENT ORGANIZERO.R. Concepts, Inc.K912834SHUR-GRIPInman Medical Corp.

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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