BASHIR Endovascular Catheter Ref. No. 7201, BASHIR S-B Endovascular Catheter, Ref. No. 7101
K-Number: K222095 · 2023-04-20
Device Summary
Frequently Asked Questions
What is the BASHIR Endovascular Catheter Ref. No. 7201, BASHIR S-B Endovascular Catheter, Ref. No. 7101?
BASHIR Endovascular Catheter Ref. No. 7201, BASHIR S-B Endovascular Catheter, Ref. No. 7101 is a medical device that received FDA 510(k) clearance on 2023-04-20. It is manufactured by Thrombolex, Inc.. The 510(k) number is K222095.
When was BASHIR Endovascular Catheter Ref. No. 7201, BASHIR S-B Endovascular Catheter, Ref. No. 7101 approved by the FDA?
BASHIR Endovascular Catheter Ref. No. 7201, BASHIR S-B Endovascular Catheter, Ref. No. 7101 received FDA 510(k) clearance on 2023-04-20, under approval number K222095.
What company makes BASHIR Endovascular Catheter Ref. No. 7201, BASHIR S-B Endovascular Catheter, Ref. No. 7101?
BASHIR Endovascular Catheter Ref. No. 7201, BASHIR S-B Endovascular Catheter, Ref. No. 7101 is manufactured by Thrombolex, Inc..
What is the FDA product code for BASHIR Endovascular Catheter Ref. No. 7201, BASHIR S-B Endovascular Catheter, Ref. No. 7101?
The FDA product code for BASHIR Endovascular Catheter Ref. No. 7201, BASHIR S-B Endovascular Catheter, Ref. No. 7101 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.