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FDA 510(k)

DUODERM TRANSPARENT HYDROCOLLOID DRESSING

K-Number: K925992 · 1993-10-15

ApplicantConvatec, A Division of E.R. Squibb & Sons
Decision Date1993-10-15
Product CodeKMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DUODERM TRANSPARENT HYDROCOLLOID 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 1993-10-15 under 510(k) number K925992. The device is classified under product code KMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUODERM TRANSPARENT HYDROCOLLOID DRESSING?

DUODERM TRANSPARENT HYDROCOLLOID DRESSING is a medical device that received FDA 510(k) clearance on 1993-10-15. The listed applicant is Convatec, A Division of E.R. Squibb & Sons. The 510(k) number is K925992.

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

DUODERM TRANSPARENT HYDROCOLLOID DRESSING received FDA 510(k) clearance on 1993-10-15, under 510(k) number K925992.

Who is the listed applicant for DUODERM TRANSPARENT HYDROCOLLOID 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 TRANSPARENT HYDROCOLLOID DRESSING?

The FDA product code for DUODERM TRANSPARENT HYDROCOLLOID DRESSING is KMK.

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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: KMK)

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.

K180994SecurAcath 10F, SecurAcath 12F, SecurAcath 5F, SecurAcath 5F, SecurAcath 6F, SecurAcath 7F/SecurAcath 8FInterrad Medical, Inc.K981860A P HARNESSParaworks Enterprise, Ltd.K963365MULTI-PURPOSE MEDICAL TUBE HOLDERByrd Medical Devices, Inc.K941098SECURE-SITEOp-Co Medical Products , Ltd.K943147STATLOCK CVVenetec, Inc.K943047IV START KITSSterile Concepts, 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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