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FDA 510(k)

BASHIR Endovascular Catheter Ref. No. 7201, BASHIR S-B Endovascular Catheter, Ref. No. 7101

K-Number: K222095 · 2023-04-20

Decision Date2023-04-20
Product CodeQEY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BASHIR Endovascular Catheter Ref. No. 7201, BASHIR S-B Endovascular Catheter, Ref. No. 7101 is a medical device manufactured by Thrombolex, Inc.. It received FDA 510(k) clearance on 2023-04-20 under approval number K222095. 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 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.

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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.