EXTERNAL INCONTINENCE CATHETER TRAVEL
K-Number: K832106 · 1983-07-19
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Device Summary
Frequently Asked Questions
What is the EXTERNAL INCONTINENCE CATHETER TRAVEL?
EXTERNAL INCONTINENCE CATHETER TRAVEL is a medical device that received FDA 510(k) clearance on 1983-07-19. The listed applicant is Plasco, Inc.. The 510(k) number is K832106.
When did EXTERNAL INCONTINENCE CATHETER TRAVEL receive FDA 510(k) clearance?
EXTERNAL INCONTINENCE CATHETER TRAVEL received FDA 510(k) clearance on 1983-07-19, under 510(k) number K832106.
Who is the listed applicant for EXTERNAL INCONTINENCE CATHETER TRAVEL?
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 TRAVEL?
The FDA product code for EXTERNAL INCONTINENCE CATHETER TRAVEL 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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