Medtronic Blood Systems, Inc.
Medtronic Blood Systems, Inc. holds FDA 510(k) medical device clearances, first cleared 1988, most recent 1995.
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.