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FDA 510(k)

CONVEEN SELF-SEALING URISHEATH MALE EXTERNAL CATH

K-Number: K854580 · 1985-12-13

ApplicantColoplast A/S
Decision Date1985-12-13
Product CodeKNX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CONVEEN SELF-SEALING URISHEATH MALE EXTERNAL CATH is the device name listed in this FDA 510(k) record. The listed applicant is Coloplast A/S. It received FDA 510(k) clearance on 1985-12-13 under 510(k) number K854580. 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 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.

View all 66 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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