Baxter Edwards
Baxter Edwards holds FDA 510(k) medical device clearances, first cleared 1993, most recent 2000.
Top product codes for Baxter Edwards
Recent clearances by Baxter Edwards
- K993816 — BAXTER PERCUTANEOUS MECHANICAL THROMBECTOMY (PMT) DEVICE, MODELS PMT0606FD AND PMT1206FD
- K981909 — BAXTER HEMOSTASIS VALVE INTRODUCERS
- K980487 — CARPENTER-EDWARDS CLASSIC RING WITH DURAFLO TREATMENT MODELS 4425 (MITRAL) AND 4525 (TRICUSPID), CARPENTER-EDWARDS PHYSM
- K965137 — FOGARTY VALVULOTOME MODEL 700091
- K964021 — INTRAMED SIDE BRANCH OCCLUSION (SBO) SYSTEM (700095 AND 700099)
- K955839 — MULTI-MED MULTI-LUMEN CENTRAL VENOUS CATHETER
- K952638 — 4.5F IMAGECATH CORONARY ANGIOSCOPE, MODEL COV45 [SUBSEQUENTLY REFERRED TO AS THE MODIFIED ANGIOSCOPE[
- K944214 — BAXTER HANDLE MODEL 1150
- K944858 — BAXTER EPTFE EXTERNALLY SUPPORTED VASCULAR GRAFTS
- K940795 — SWAN-GANZ CC0/SVO2 THERMODILUTION CATHETER
- K926433 — 4.5F IMAGECATH(R) CORONARY ANGIOSCOPE, COV45
Data sourced from openFDA. This site is unofficial and independent of the FDA.