ClearanceBrief
510(k) K232679 · QEW Peripheral Mechanical Thrombectomy With Aspiration

Cleaner™ Pro Thrombectomy System; Cleaner™ Pro Aspiration Catheter with Handpiece; Cleaner™ Pro Aspiration Canister

ApplicantArgon Medical Devices, Inc., Athens TX, US
DecisionSubstantially Equivalent, Jan 19, 2024
ReceivedSep 1, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K232679

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.