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FDA 510(k)

DUODERM HYDROACTIVE DRESSING AND CGF DRESSINGS

K-Number: K912667 · 1991-09-04

ApplicantConvatec, A Division of E.R. Squibb & Sons
Decision Date1991-09-04
Product CodeMGQ
DecisionSubstantially Equivalent

Device Summary

DUODERM HYDROACTIVE DRESSING AND CGF DRESSINGS 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 1991-09-04 under 510(k) number K912667. The device is classified under product code MGQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUODERM HYDROACTIVE DRESSING AND CGF DRESSINGS?

DUODERM HYDROACTIVE DRESSING AND CGF DRESSINGS is a medical device that received FDA 510(k) clearance on 1991-09-04. The listed applicant is Convatec, A Division of E.R. Squibb & Sons. The 510(k) number is K912667.

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

DUODERM HYDROACTIVE DRESSING AND CGF DRESSINGS received FDA 510(k) clearance on 1991-09-04, under 510(k) number K912667.

Who is the listed applicant for DUODERM HYDROACTIVE DRESSING AND CGF DRESSINGS?

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 AND CGF DRESSINGS?

The FDA product code for DUODERM HYDROACTIVE DRESSING AND CGF DRESSINGS is MGQ.

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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: MGQ)

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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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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