Medtronic Bio-Medicus, Inc.
Medtronic Bio-Medicus, Inc. holds FDA 510(k) medical device clearances, first cleared 1992, most recent 1998.
Top product codes for Medtronic Bio-Medicus, Inc.
Recent clearances by Medtronic Bio-Medicus, Inc.
- K973237 — CSS-CARDIOPLEGIA SAFETY SYSTEM
- K973011 — BPX80 BIO-PUMP (BPX80)
- K954501 — BIOTREND OXYGEN SATURATION & HEMATOCRIT SYSTEM
- K941922 — MEDSAT OXYGEN SATURATION SYSTEM
- K936091 — MEDTRONIC BIO-MEDICUS BIO-CONSOLE MODEL 550M PUMP SPEED CONTROLLER
- K941921 — BIO-MEDICUS BIO-CONSOLE MODELS 540, 540A,B,C,D,E, & 550
- K924208 — BIO-PROBE(R) BLOOD FLOW MONITORING SYST(TX-50/50P)
- K926357 — MEDTRONIC BIO-MEDICUS HANDCRANK MODEL 150
- K924206 — MEDTRONIC BIO-MEDICUS BIO-CONSOLE MODEL 540E
- K924205 — MEDTRONIC BIO-MEDICUS BIO-CONSOLE MODEL 550
- K924642 — MEDTRONIC BIO-MEDICUS FEMORAL CANNULA/INTRODUCER
- K924643 — MEDTRONIC BIO-MEDICUS CANNULA INSERTION KIT
- K914754 — MEDTRONIC BIO-MEDICUS BIO-CONSOLE MODEL 540-D
Data sourced from openFDA. This site is unofficial and independent of the FDA.