Medtronic Blood Systems, Inc.
FDA 510(k) medical device clearances.
Top product codes for Medtronic Blood Systems, Inc.
Recent clearances by Medtronic Blood Systems, Inc.
- K944957 — TEMPORARY MYOCARDIAL PACING LEAD, MODEL 6500
- K944966 — UNIPOLAR ATRIAL TEMPORARY PACING LEAD,MODEL 6492
- K893207 — CLOSED CHEST SUPPORT CIRCUIT
- K893678 — DURAN FLEXIBLE ANNULOPLASTY RING & OBTURATOR H601H
- K891687 — EXTRACORPOREAL CIRCUIT WITH BIO-ACTIVE SURFACE
- K891230 — MAXIMA* HOLLOW FIBER OXYGENATOR W/FILTERED RESERV.
- K885154 — INTERSEPT* CRYSTALLOID CARDIOPLEGIA DELIV. SYSTEM
- K884390 — INTERSEPT* CRYSTALLOID CARDIOPLEGIA FILTER
- K884244 — INTERSEPT* PREBYPASS FILTER
- K883439 — INTERSEPT*CRYSTALLOID CARDIOPLEGIA DELIVERY SYSTEM
- K883086 — INTERSEPT*PREBYPASS FILTER
- K882137 — EXTENDED SHELF LIFE FOR INTERSEPT* ARTERIAL 20/40
- K882136 — INTERSEPT* OXYGEN GAS LINE FILTER
- K882479 — 26MM DIAMETER HANCOCK* TROCAR BLADE AND TIP
- K880671 — MODIFIED INTERSEPT PEDIATRIC BLOOD FILTER
Data sourced from openFDA. This site is unofficial and independent of the FDA.