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FDA 510(k)

CONVEEN LEG BAG W/TUBE-DRAINAGE BAG

K-Number: K832537 · 1983-09-12

Decision Date1983-09-12
Product CodeKNX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CONVEEN LEG BAG W/TUBE-DRAINAGE BAG 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 1983-09-12 under 510(k) number K832537. 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 LEG BAG W/TUBE-DRAINAGE BAG?

CONVEEN LEG BAG W/TUBE-DRAINAGE BAG is a medical device that received FDA 510(k) clearance on 1983-09-12. The listed applicant is Telcam Medical Devices, Inc.. The 510(k) number is K832537.

When did CONVEEN LEG BAG W/TUBE-DRAINAGE BAG receive FDA 510(k) clearance?

CONVEEN LEG BAG W/TUBE-DRAINAGE BAG received FDA 510(k) clearance on 1983-09-12, under 510(k) number K832537.

Who is the listed applicant for CONVEEN LEG BAG W/TUBE-DRAINAGE BAG?

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 LEG BAG W/TUBE-DRAINAGE BAG?

The FDA product code for CONVEEN LEG BAG W/TUBE-DRAINAGE BAG 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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