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FDA 510(k)

COMPEED PSORIASIS DRESSING

K-Number: K982493 · 1999-01-28

ApplicantColoplast Corp.
Decision Date1999-01-28
Product CodeFRO
DecisionSubstantially Equivalent

Device Summary

COMPEED PSORIASIS DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Coloplast Corp.. It received FDA 510(k) clearance on 1999-01-28 under 510(k) number K982493. 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 COMPEED PSORIASIS DRESSING?

COMPEED PSORIASIS DRESSING is a medical device that received FDA 510(k) clearance on 1999-01-28. The listed applicant is Coloplast Corp.. The 510(k) number is K982493.

When did COMPEED PSORIASIS DRESSING receive FDA 510(k) clearance?

COMPEED PSORIASIS DRESSING received FDA 510(k) clearance on 1999-01-28, under 510(k) number K982493.

Who is the listed applicant for COMPEED PSORIASIS DRESSING?

The FDA 510(k) record lists Coloplast Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COMPEED PSORIASIS DRESSING?

The FDA product code for COMPEED PSORIASIS DRESSING is FRO. This falls under the Anesthesiology category.

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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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