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FDA 510(k)

LAP SPONGES, MODIFIED

K-Number: K913303 · 1992-08-06

ApplicantCarwild Corp.
Decision Date1992-08-06
Product CodeGDY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LAP SPONGES, MODIFIED is the device name listed in this FDA 510(k) record. The listed applicant is Carwild Corp.. It received FDA 510(k) clearance on 1992-08-06 under 510(k) number K913303. 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 LAP SPONGES, MODIFIED?

LAP SPONGES, MODIFIED is a medical device that received FDA 510(k) clearance on 1992-08-06. The listed applicant is Carwild Corp.. The 510(k) number is K913303.

When did LAP SPONGES, MODIFIED receive FDA 510(k) clearance?

LAP SPONGES, MODIFIED received FDA 510(k) clearance on 1992-08-06, under 510(k) number K913303.

Who is the listed applicant for LAP SPONGES, MODIFIED?

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

What is the FDA product code for LAP SPONGES, MODIFIED?

The FDA product code for LAP SPONGES, MODIFIED is GDY.

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 Carwild 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.

K913302DISPOSABLE SPECIALTY SPONGES (DISSECTORS)/MODIFIEDK833688SUTURE REMOVAL KITS STERILEK791872LAP SPONGESK791870DISPOSABLE SPECIALITY SPONGESK791871NEUROLOGICAL SPONGES (PATTIES)

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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