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FDA 510(k)

DUODERM(R) CGF

K-Number: K881050 · 1988-04-01

ApplicantConvatec, A Division of E.R. Squibb & Sons
Decision Date1988-04-01
Product CodeNAD
Advisory CommitteeSU
DecisionSubstantially Equivalent for Some Indications

Device Summary

DUODERM(R) CGF 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 1988-04-01 under 510(k) number K881050. The device is classified under product code NAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the DUODERM(R) CGF?

DUODERM(R) CGF is a medical device that received FDA 510(k) clearance on 1988-04-01. The listed applicant is Convatec, A Division of E.R. Squibb & Sons. The 510(k) number is K881050.

When did DUODERM(R) CGF receive FDA 510(k) clearance?

DUODERM(R) CGF received FDA 510(k) clearance on 1988-04-01, under 510(k) number K881050.

Who is the listed applicant for DUODERM(R) CGF?

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(R) CGF?

The FDA product code for DUODERM(R) CGF is NAD.

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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: NAD)

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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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