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FDA 510(k)

Bashir Endovascular Catheter Model 7201, Bashir N-X Endovascular Catheter, Mode 7200

K-Number: K183290 · 2019-02-25

Decision Date2019-02-25
Product CodeQEY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Bashir Endovascular Catheter Model 7201, Bashir N-X Endovascular Catheter, Mode 7200 is a medical device manufactured by Thrombolex, Inc.. It received FDA 510(k) clearance on 2019-02-25 under approval number K183290. The device is classified under product code QEY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Bashir Endovascular Catheter Model 7201, Bashir N-X Endovascular Catheter, Mode 7200?

Bashir Endovascular Catheter Model 7201, Bashir N-X Endovascular Catheter, Mode 7200 is a medical device that received FDA 510(k) clearance on 2019-02-25. It is manufactured by Thrombolex, Inc.. The 510(k) number is K183290.

When was Bashir Endovascular Catheter Model 7201, Bashir N-X Endovascular Catheter, Mode 7200 approved by the FDA?

Bashir Endovascular Catheter Model 7201, Bashir N-X Endovascular Catheter, Mode 7200 received FDA 510(k) clearance on 2019-02-25, under approval number K183290.

What company makes Bashir Endovascular Catheter Model 7201, Bashir N-X Endovascular Catheter, Mode 7200?

Bashir Endovascular Catheter Model 7201, Bashir N-X Endovascular Catheter, Mode 7200 is manufactured by Thrombolex, Inc..

What is the FDA product code for Bashir Endovascular Catheter Model 7201, Bashir N-X Endovascular Catheter, Mode 7200?

The FDA product code for Bashir Endovascular Catheter Model 7201, Bashir N-X Endovascular Catheter, Mode 7200 is QEY.

Related Clinical Trials

Other Devices by Thrombolex, Inc.

Related Devices (Code: QEY)

Official Source

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