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FDA 510(k)

DERMATOLOGICAL PATCH

K-Number: K872926 · 1988-02-22

ApplicantConvatec, A Division of E.R. Squibb & Sons
Decision Date1988-02-22
Product CodeFRO
DecisionSubstantially Equivalent for Some Indications

Device Summary

DERMATOLOGICAL PATCH 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 1988-02-22 under 510(k) number K872926. 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 for Some Indications.

Frequently Asked Questions

What is the DERMATOLOGICAL PATCH?

DERMATOLOGICAL PATCH is a medical device that received FDA 510(k) clearance on 1988-02-22. The listed applicant is Convatec, A Division of E.R. Squibb & Sons. The 510(k) number is K872926.

When did DERMATOLOGICAL PATCH receive FDA 510(k) clearance?

DERMATOLOGICAL PATCH received FDA 510(k) clearance on 1988-02-22, under 510(k) number K872926.

Who is the listed applicant for DERMATOLOGICAL PATCH?

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 DERMATOLOGICAL PATCH?

The FDA product code for DERMATOLOGICAL PATCH is FRO. This falls under the Anesthesiology category.

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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.

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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.

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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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