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FDA 510(k)

CONVEEN URISHEATH & CONVEEN URILINER

K-Number: K812294 · 1981-08-31

Decision Date1981-08-31
Product CodeKNX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CONVEEN URISHEATH & CONVEEN URILINER is the device name listed in this FDA 510(k) record. The listed applicant is Telcam Medical Devices, Inc.. It received FDA 510(k) clearance on 1981-08-31 under 510(k) number K812294. 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 URISHEATH & CONVEEN URILINER?

CONVEEN URISHEATH & CONVEEN URILINER is a medical device that received FDA 510(k) clearance on 1981-08-31. The listed applicant is Telcam Medical Devices, Inc.. The 510(k) number is K812294.

When did CONVEEN URISHEATH & CONVEEN URILINER receive FDA 510(k) clearance?

CONVEEN URISHEATH & CONVEEN URILINER received FDA 510(k) clearance on 1981-08-31, under 510(k) number K812294.

Who is the listed applicant for CONVEEN URISHEATH & CONVEEN URILINER?

The FDA 510(k) record lists Telcam Medical Devices, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONVEEN URISHEATH & CONVEEN URILINER?

The FDA product code for CONVEEN URISHEATH & CONVEEN URILINER 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 Telcam Medical Devices, 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

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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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