CONVEEN SELF-SEALING URISHEATH MALE EXTERNAL CATH
K-Number: K854580 · 1985-12-13
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Device Summary
Frequently Asked Questions
What is the CONVEEN SELF-SEALING URISHEATH MALE EXTERNAL CATH?
CONVEEN SELF-SEALING URISHEATH MALE EXTERNAL CATH is a medical device that received FDA 510(k) clearance on 1985-12-13. The listed applicant is Coloplast A/S. The 510(k) number is K854580.
When did CONVEEN SELF-SEALING URISHEATH MALE EXTERNAL CATH receive FDA 510(k) clearance?
CONVEEN SELF-SEALING URISHEATH MALE EXTERNAL CATH received FDA 510(k) clearance on 1985-12-13, under 510(k) number K854580.
Who is the listed applicant for CONVEEN SELF-SEALING URISHEATH MALE EXTERNAL CATH?
The FDA 510(k) record lists Coloplast A/S as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CONVEEN SELF-SEALING URISHEATH MALE EXTERNAL CATH?
The FDA product code for CONVEEN SELF-SEALING URISHEATH MALE EXTERNAL CATH 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 Coloplast A/S 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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