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FDA 510(k)

DISP. SKIN STAPLER REMOVALBLE SKINSTAPLE

K-Number: K821024 · 1982-05-14

ApplicantHowmedica Corp.
Decision Date1982-05-14
Product CodeGDT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DISP. SKIN STAPLER REMOVALBLE SKINSTAPLE is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1982-05-14 under 510(k) number K821024. The device is classified under product code GDT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISP. SKIN STAPLER REMOVALBLE SKINSTAPLE?

DISP. SKIN STAPLER REMOVALBLE SKINSTAPLE is a medical device that received FDA 510(k) clearance on 1982-05-14. The listed applicant is Howmedica Corp.. The 510(k) number is K821024.

When did DISP. SKIN STAPLER REMOVALBLE SKINSTAPLE receive FDA 510(k) clearance?

DISP. SKIN STAPLER REMOVALBLE SKINSTAPLE received FDA 510(k) clearance on 1982-05-14, under 510(k) number K821024.

Who is the listed applicant for DISP. SKIN STAPLER REMOVALBLE SKINSTAPLE?

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

What is the FDA product code for DISP. SKIN STAPLER REMOVALBLE SKINSTAPLE?

The FDA product code for DISP. SKIN STAPLER REMOVALBLE SKINSTAPLE is GDT.

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Other records listing Howmedica Corp. 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.

K983528MICRO DYNAMIC MESHK983404TYPE 3 FEMORAL COMPONENTSK980926DURATION II ACETABULAR COMPONENTS-ETHYLENE OXIDE STERILIZATIONK980925DURATION II TIBIAL INSERTS-ETHYLENE OXIDE STERILIZATIONK980626DURATION II ACETABULAR COMPONENTS-GAS PLASMA STERILIZATIONK980632DURATION II TIBIAL INSERTS - GAS PLASMA STERILIZATION

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Related Devices (Code: GDT)

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.

K963234STAPLE REMOVAL KITContinental Medical Laboratories, Inc.K943719VISISTAT STAPLERPilling Weck, Inc.K925526MANIPLER DISPOSABLE SKIN STAPLERMatsutani Seisakusho Co. , Ltd.K915430SKIN STAPLE REMOVER KITCypress Medical Products, Ltd.K911204QUALTEX SKIN STAPLE EXTRACTORDeroyal Industries, Inc.K910586AUTO SUTURE(R) POLYMER SKIN GRAFT STAPLER*United States Surgical, A Division of Tyco Healthc

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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