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FDA 510(k)

CHESEBROUGH-POND'S REUSABLE URINARY LEG

K-Number: K842553 · 1984-07-20

Decision Date1984-07-20
Product CodeKNX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CHESEBROUGH-POND'S REUSABLE URINARY LEG 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 1984-07-20 under 510(k) number K842553. The device is classified under product code KNX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHESEBROUGH-POND'S REUSABLE URINARY LEG?

CHESEBROUGH-POND'S REUSABLE URINARY LEG is a medical device that received FDA 510(k) clearance on 1984-07-20. The listed applicant is Chesebrough-Pond'S U.S.A. Co.. The 510(k) number is K842553.

When did CHESEBROUGH-POND'S REUSABLE URINARY LEG receive FDA 510(k) clearance?

CHESEBROUGH-POND'S REUSABLE URINARY LEG received FDA 510(k) clearance on 1984-07-20, under 510(k) number K842553.

Who is the listed applicant for CHESEBROUGH-POND'S REUSABLE URINARY LEG?

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 REUSABLE URINARY LEG?

The FDA product code for CHESEBROUGH-POND'S REUSABLE URINARY LEG is KNX.

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: KNX)

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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