Thrombolex, Inc.
Thrombolex, Inc. holds FDA 510(k) medical device clearances, first cleared 2019, most recent 2023.
Top product codes for Thrombolex, Inc.
Recent clearances by Thrombolex, Inc.
- K231653 — BASHIR .035 Endovascular Catheter, BASHIR S-B .035 Endovascular Catheter
- K222095 — BASHIR Endovascular Catheter Ref. No. 7201, BASHIR S-B Endovascular Catheter, Ref. No. 7101
- K211061 — 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)
- K193071 — Bashir Plus Endovascular Catheter
- K192598 — Bashir S-B Endovascular Catheter, Ref. No. 7101
- K183290 — Bashir Endovascular Catheter Model 7201, Bashir N-X Endovascular Catheter, Mode 7200
Data sourced from openFDA. This site is unofficial and independent of the FDA.