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FDA 510(k)

COMBIDERM ACD

K-Number: K954918 · 1995-12-26

ApplicantConvatec, A Bristol-Myers Squibb Co.
Decision Date1995-12-26
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

COMBIDERM ACD is the device name listed in this FDA 510(k) record. The listed applicant is Convatec, A Bristol-Myers Squibb Co.. It received FDA 510(k) clearance on 1995-12-26 under 510(k) number K954918. The device is classified under product code KMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMBIDERM ACD?

COMBIDERM ACD is a medical device that received FDA 510(k) clearance on 1995-12-26. The listed applicant is Convatec, A Bristol-Myers Squibb Co.. The 510(k) number is K954918.

When did COMBIDERM ACD receive FDA 510(k) clearance?

COMBIDERM ACD received FDA 510(k) clearance on 1995-12-26, under 510(k) number K954918.

Who is the listed applicant for COMBIDERM ACD?

The FDA 510(k) record lists Convatec, A Bristol-Myers Squibb Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COMBIDERM ACD?

The FDA product code for COMBIDERM ACD is KMF.

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Other records listing Convatec, A Bristol-Myers Squibb Co. 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.

K032734CONVATEC FECAL MANAGEMENT SYSTEMK990368DUODERM HYDROACTIVE GEL WOUND DRESSINGK982116AQUACEL HYDROFIBER WOUND DRESSINGK973806DUODERM HYDROACTIVE GELK973807DUODERM HYDROACTIVE PASTEK973717COMBIDERM ACD

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Related Devices (Code: KMF)

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.

K241916TearRepair Liquid Skin ProtectantOptmed, Inc.K182733Rochal Bioshield Silicone FilmRochal Industries, LLCK171148Aleo BME Liquid BandageAleo Bme, Inc.K153571Cavilon Advanced High Endurance Skin Protectant3M HealthcareK160684Atteris No-Sting Skin ProtectantRochal Industries, LLCK120059LIQUID BANDAGEChesson Laboratory Associates, 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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