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FDA 510(k)

CHESEBROUGH POND'S HYDROCOLLOID DRESSING

K-Number: K862803 · 1986-11-14

Decision Date1986-11-14
Product CodeFRO
DecisionSubstantially Equivalent for Some Indications

Device Summary

CHESEBROUGH POND'S HYDROCOLLOID DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Chesebrough-Pond'S U.S.A. Co.. It received FDA 510(k) clearance on 1986-11-14 under 510(k) number K862803. 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 CHESEBROUGH POND'S HYDROCOLLOID DRESSING?

CHESEBROUGH POND'S HYDROCOLLOID DRESSING is a medical device that received FDA 510(k) clearance on 1986-11-14. The listed applicant is Chesebrough-Pond'S U.S.A. Co.. The 510(k) number is K862803.

When did CHESEBROUGH POND'S HYDROCOLLOID DRESSING receive FDA 510(k) clearance?

CHESEBROUGH POND'S HYDROCOLLOID DRESSING received FDA 510(k) clearance on 1986-11-14, under 510(k) number K862803.

Who is the listed applicant for CHESEBROUGH POND'S HYDROCOLLOID DRESSING?

The FDA 510(k) record lists Chesebrough-Pond'S U.S.A. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CHESEBROUGH POND'S HYDROCOLLOID DRESSING?

The FDA product code for CHESEBROUGH POND'S HYDROCOLLOID DRESSING 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 Chesebrough-Pond'S U.S.A. Co. 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.

View all 33 devices →

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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