CHESEBROUGH-POND'S REUSABLE URINARY LEG
K-Number: K842553 · 1984-07-20
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Device Summary
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.
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
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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