DUODERM FLEXIBLE HYDROACTIVE DRESSINGS
K-Number: K821656 · 1982-09-07
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Device Summary
Frequently Asked Questions
What is the DUODERM FLEXIBLE HYDROACTIVE DRESSINGS?
DUODERM FLEXIBLE HYDROACTIVE DRESSINGS is a medical device that received FDA 510(k) clearance on 1982-09-07. The listed applicant is Convatec, A Division of E.R. Squibb & Sons. The 510(k) number is K821656.
When did DUODERM FLEXIBLE HYDROACTIVE DRESSINGS receive FDA 510(k) clearance?
DUODERM FLEXIBLE HYDROACTIVE DRESSINGS received FDA 510(k) clearance on 1982-09-07, under 510(k) number K821656.
Who is the listed applicant for DUODERM FLEXIBLE HYDROACTIVE 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 FLEXIBLE HYDROACTIVE DRESSINGS?
The FDA product code for DUODERM FLEXIBLE HYDROACTIVE DRESSINGS is FRO. This falls under the Anesthesiology category.
Related Clinical Trials
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.
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.
Related Devices (Code: FRO)
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.
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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