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FDA 510(k)

DUODERM HYDROACTIVE DRESSING

K-Number: K925993 · 1993-10-28

ApplicantConvatec, A Division of E.R. Squibb & Sons
Decision Date1993-10-28
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent for Some Indications

Device Summary

DUODERM HYDROACTIVE DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Convatec, A Division of E.R. Squibb & Sons. It received FDA 510(k) clearance on 1993-10-28 under 510(k) number K925993. The device is classified under product code KMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the DUODERM HYDROACTIVE DRESSING?

DUODERM HYDROACTIVE DRESSING is a medical device that received FDA 510(k) clearance on 1993-10-28. The listed applicant is Convatec, A Division of E.R. Squibb & Sons. The 510(k) number is K925993.

When did DUODERM HYDROACTIVE DRESSING receive FDA 510(k) clearance?

DUODERM HYDROACTIVE DRESSING received FDA 510(k) clearance on 1993-10-28, under 510(k) number K925993.

Who is the listed applicant for DUODERM HYDROACTIVE DRESSING?

The FDA 510(k) record lists Convatec, A Division of E.R. Squibb & Sons as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DUODERM HYDROACTIVE DRESSING?

The FDA product code for DUODERM HYDROACTIVE DRESSING is KMF.

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Other records listing Convatec, A Division of E.R. Squibb & Sons 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.

K013814ABSORBENT ANTIMICROBIAL WOUND DRESSINGK990964SIGNADRESS DUODERM DRESSINGK984388HA ABSORBENT WOUND DRESSINGK980720NONWOVEN PADK980382NON-WOVEN COMPRESSK974823NONWOVEN DRESSING

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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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