Bashir Endovascular Catheter Model 7201, Bashir N-X Endovascular Catheter, Mode 7200
K-Number: K183290 · 2019-02-25
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.