EXTERNAL INCONTINENCE CATHETER SET-NON
K-Number: K832108 · 1983-07-18
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Device Summary
Frequently Asked Questions
What is the EXTERNAL INCONTINENCE CATHETER SET-NON?
EXTERNAL INCONTINENCE CATHETER SET-NON is a medical device that received FDA 510(k) clearance on 1983-07-18. The listed applicant is Plasco, Inc.. The 510(k) number is K832108.
When did EXTERNAL INCONTINENCE CATHETER SET-NON receive FDA 510(k) clearance?
EXTERNAL INCONTINENCE CATHETER SET-NON received FDA 510(k) clearance on 1983-07-18, under 510(k) number K832108.
Who is the listed applicant for EXTERNAL INCONTINENCE CATHETER SET-NON?
The FDA 510(k) record lists Plasco, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EXTERNAL INCONTINENCE CATHETER SET-NON?
The FDA product code for EXTERNAL INCONTINENCE CATHETER SET-NON 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 Plasco, Inc. 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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