DUODERM(R) HYDROACTIVE(R) PASTE
K-Number: K881302 · 1988-04-28
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Device Summary
Frequently Asked Questions
What is the DUODERM(R) HYDROACTIVE(R) PASTE?
DUODERM(R) HYDROACTIVE(R) PASTE is a medical device that received FDA 510(k) clearance on 1988-04-28. The listed applicant is Convatec, A Division of E.R. Squibb & Sons. The 510(k) number is K881302.
When did DUODERM(R) HYDROACTIVE(R) PASTE receive FDA 510(k) clearance?
DUODERM(R) HYDROACTIVE(R) PASTE received FDA 510(k) clearance on 1988-04-28, under 510(k) number K881302.
Who is the listed applicant for DUODERM(R) HYDROACTIVE(R) PASTE?
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) HYDROACTIVE(R) PASTE?
The FDA product code for DUODERM(R) HYDROACTIVE(R) PASTE 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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