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FDA 510(k)

DUODERM DRESSINGS, CGF DRESSINGS, PASTE FULL THICK

K-Number: K904852 · 1991-01-25

Decision Date1991-01-25
Product CodeFRO
DecisionSubstantially Equivalent

Device Summary

DUODERM DRESSINGS, CGF DRESSINGS, PASTE FULL THICK 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 1991-01-25 under 510(k) number K904852. The device is classified under product code FRO. Product code FRO falls under the category of Anesthesiology, which includes devices for anesthetic delivery and patient monitoring. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUODERM DRESSINGS, CGF DRESSINGS, PASTE FULL THICK?

DUODERM DRESSINGS, CGF DRESSINGS, PASTE FULL THICK is a medical device that received FDA 510(k) clearance on 1991-01-25. The listed applicant is Convatec, A Division of E.R. Squibb & Sons. The 510(k) number is K904852.

When did DUODERM DRESSINGS, CGF DRESSINGS, PASTE FULL THICK receive FDA 510(k) clearance?

DUODERM DRESSINGS, CGF DRESSINGS, PASTE FULL THICK received FDA 510(k) clearance on 1991-01-25, under 510(k) number K904852.

Who is the listed applicant for DUODERM DRESSINGS, CGF DRESSINGS, PASTE FULL THICK?

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 DRESSINGS, CGF DRESSINGS, PASTE FULL THICK?

The FDA product code for DUODERM DRESSINGS, CGF DRESSINGS, PASTE FULL THICK 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.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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