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FDA 510(k)

Selebrek PTCA Balloon Dilatation Catheter

K-Number: K211349 · 2022-01-07

Decision Date2022-01-07
Product CodeLOX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Selebrek PTCA Balloon Dilatation Catheter is a medical device manufactured by Kossel Medtech (Suzhou) Co., Ltd.. It received FDA 510(k) clearance on 2022-01-07 under approval number K211349. The device is classified under product code LOX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Selebrek PTCA Balloon Dilatation Catheter?

Selebrek PTCA Balloon Dilatation Catheter is a medical device that received FDA 510(k) clearance on 2022-01-07. It is manufactured by Kossel Medtech (Suzhou) Co., Ltd.. The 510(k) number is K211349.

When was Selebrek PTCA Balloon Dilatation Catheter approved by the FDA?

Selebrek PTCA Balloon Dilatation Catheter received FDA 510(k) clearance on 2022-01-07, under approval number K211349.

What company makes Selebrek PTCA Balloon Dilatation Catheter?

Selebrek PTCA Balloon Dilatation Catheter is manufactured by Kossel Medtech (Suzhou) Co., Ltd..

What is the FDA product code for Selebrek PTCA Balloon Dilatation Catheter?

The FDA product code for Selebrek PTCA Balloon Dilatation Catheter is LOX.

Related Clinical Trials

Other Devices by Kossel Medtech (Suzhou) Co., Ltd.

Related Devices (Code: LOX)

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.