FDA 510(k) Applications Submitted by Thrombolex, Inc.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K231653 |
06/06/2023 |
BASHIRÖ .035 Endovascular Catheter, BASHIRÖ S-B .035 Endovascular Catheter |
Thrombolex, Inc. |
| K222095 |
07/18/2022 |
BASHIR Endovascular Catheter Ref. No. 7201, BASHIR S-B Endovascular Catheter, Ref. No. 7101 |
Thrombolex, Inc. |
| K211061 |
04/09/2021 |
BASHIR Endovascular Catheter (Ref. 7201), BASHIR Plus 10 Endovascular Catheter (Ref. 7210), BASHIR Plus 20 Endovascular Catheter (Ref. 7220), BASHIR Plus 30 Endovascular Catheter (Ref. 7230), BASHIR Plus 40 Endovascular Catheter (Ref. 7240) |
Thrombolex, Inc. |
| K192598 |
09/20/2019 |
Bashir S-B Endovascular Catheter, Ref. No. 7101 |
Thrombolex, Inc. |
| K193071 |
11/04/2019 |
Bashir Plus Endovascular Catheter |
Thrombolex, Inc. |
| K183290 |
11/26/2018 |
Bashir Endovascular Catheter Model 7201, Bashir N-X Endovascular Catheter, Mode 7200 |
Thrombolex, Inc. |
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