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FDA 510(k)

LAPARATOMY SPONGE

K-Number: K781818 · 1978-11-15

ApplicantMeden Medical Sales Division
Decision Date1978-11-15
Product CodeGDY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LAPARATOMY SPONGE is the device name listed in this FDA 510(k) record. The listed applicant is Meden Medical Sales Division. It received FDA 510(k) clearance on 1978-11-15 under 510(k) number K781818. The device is classified under product code GDY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAPARATOMY SPONGE?

LAPARATOMY SPONGE is a medical device that received FDA 510(k) clearance on 1978-11-15. The listed applicant is Meden Medical Sales Division. The 510(k) number is K781818.

When did LAPARATOMY SPONGE receive FDA 510(k) clearance?

LAPARATOMY SPONGE received FDA 510(k) clearance on 1978-11-15, under 510(k) number K781818.

Who is the listed applicant for LAPARATOMY SPONGE?

The FDA 510(k) record lists Meden Medical Sales Division as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LAPARATOMY SPONGE?

The FDA product code for LAPARATOMY SPONGE is GDY.

Related Clinical Trials

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Related Devices (Code: GDY)

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.

K972634ULTRACELL SUCTION SPONGEUltracell Medical Technologies, Inc.K960236CPR LAP SPONGESCustom Pack ReliabilityK955599STRYKER FEMORAL CANAL SPONGE & ACETABULUM SPONGEStryker Corp.K955322PROTEC X-RAY DETECTABLE GAUZE SPONGEDerivados DE Gasa, S.A. DE C.V.K953830KENSORBKentron Health Care, Inc.K953059KITTNER DISSECTORMedical Perspectives 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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