Thrombolex, Inc.

Thrombolex, Inc. has submitted 6 FDA 510(k) premarket notifications since 2019, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Mechanical Thrombolysis Catheter . Use the specialty filter in the sidebar to narrow results.

BASHIR? .035 Endovascular Catheter, BASHIR? S-B .035 Endovascular Catheter

K231653 · QEY Mechanical Thrombolysis... · Cardiovascular

Jul 2023 27d

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

K222095 · QEY Mechanical Thrombolysis... · Cardiovascular

Apr 2023 276d

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)

K211061 · QEY Mechanical Thrombolysis... · Cardiovascular

Jun 2021 62d

Bashir Plus Endovascular Catheter

K193071 · QEY Mechanical Thrombolysis... · Cardiovascular

Dec 2019 43d

Bashir S-B Endovascular Catheter, Ref. No. 7101

K192598 · QEY Mechanical Thrombolysis... · Cardiovascular

Oct 2019 28d

Bashir Endovascular Catheter Model 7201, Bashir N-X Endovascular Catheter, Mode 7200

K183290 · QEY Mechanical Thrombolysis... · Cardiovascular

Feb 2019 91d

Thrombolex, Inc. — FDA 510(k) Submissions

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