Cobe Cardiovascular, Inc.
FDA 510(k) medical device clearances.
Top product codes for Cobe Cardiovascular, Inc.
Recent clearances by Cobe Cardiovascular, Inc.
- K050111 — SMARXT BMR 1900 CLOSED VENOUS RESERVOIR BAG
- K042473 — COBE ANGEL WHOLE BLOOD SEPARATION SYSTEM
- K040184 — DIDECO MICRO 40 PH.I.S.I.O. ADULT ARTERIAL FILTER
- K033641 — SMARXT VVR4000I PLUS FILTERED HARDSHELL VENOUS RESERVOIR, MODEL 439914800
- K030462 — COBE REVOLUTION CENTRIFUGAL BLOOD PUMP WITH PC, MODEL 050300700
- K021830 — SORIN BIOMEDICA SMARXT BCD VANGUARD SURFACE MODIFIED CARDIOPLEGIA SYSTEM
- K011835 — COBE REVOLUTION
- K013480 — COBE SMARXT OPTIMIN SURFACE MODIFIED HOLLOW FIBER MEMBRANE OXYGENATOR
- K012763 — SORIN BIOMEDICA SMART BCD VANGUARD,SURFACE MODIFIED BLOOD CARDIOPLEGIA SYSTEM
- K001509 — STOCKERT V172 SERIES VENOUS FEMORAL CANNULAE
- K012898 — MODIFICATION TO: CSC14 BLOOD CARDIOPLEGIA SYSTEM
- K004046 — COBE VVR 4000 FILTERED HARDSHELL VENOUS RESERVOIR, COBE SMARXT VVR 4000 FILTERED HARDSHELL VENOUS RESERVOIR
- K002493 — DIDECO MICRO 40 PH.I.S.I.O (PHOSPHORYLCHOLINE INSERT SURFACE IN OXGENATION) NEWBORN/INFANT ARTERIAL FILTER
- K002591 — COBE SMARXT VVR 4000 FILTERED HARDSHELL VENOUS RESERVOIR
- K994209 — STOCKERT V142 SERIES VENOUS CANNULAE WITH LIGHTHOUSE TIP
- K000255 — COBE SMARXT OPTIMA XP SURFACE MODIFIED HOLLOW FIBER MEMBRANE OXYGENATOR
- K994389 — COBE HVR 2200 HARDSHELL VENOUS RESERVOIR, FILTERED
- K993001 — COBE SMARXT HVR 4000 SURFACE MODIFIED HARDSHELL VENOUS RESERVOIR, FILTERED & NONFILTERED
- K991452 — COBE OPTIMIN HOLLOW FIBER MEMBRANE OXYGENATOR
- K991986 — COBE BRAT 2 AUTOLOGOUS BLOOD SALVAGE SYSTEM WITH THE CRIT-LINE HEMATOCRIT SAMPLING SYSTEM OPTION
- K990239 — COBE VVR 4000 FILTERED HARDSHELL VENOUS RESERVOIR
- K984456 — COBE HVR 4000 FILTERED HARDSHELL VENOUS RESERVOIR
- K981613 — COBE SMARXT TUBING AND CONNECTORS
- K982406 — COBE VACUUM RELIEF CHECK VALVE
- K982254 — COBE SENTRY SMARXT 43 MICRON ARTERIAL FILTER WITH PRIMEGARD
- K980786 — COBE CLOSED VENOUS RESERVOIR BAGS WITH SMARX T, MODELS VRB 1200 AND VRB 1800
- K974812 — COBE(R) CML DUO(R) WITH SMART(TM) SURFACE MODIFIED MEMBRANCE OXYGENATOR
- K974897 — COBE BRAT 2 SYSTEM WITH MODIFIED STANDARD VOLUME PROCESSING SET
- K974085 — COBE OXYGENATOR PRODUCTS
- K963518 — COBE OPTIMA XP HOLLOW FIBER MEMBRANE OXYGENATOR
- K973627 — STANDARD VOLUME PROCESSING SET FOR THE COBE BRAT 2 AUTOLOGOUS BLOOD SALVAGE SYSTEM
- K964043 — COBE OPTIMA AND COBE CML DUO MEMBRANE OXYGENATORS
- K971669 — COBE HVR 4000 FILTERED AND NONFILTERED HARDSHELL VENOUS RESERVOIR
- K960974 — COBE CENTURY PERFUSION PUMP
- K962689 — COBE BRAT 2 AUTOLOGOUS BLOOD SALVAGE SYSTEM WITH MODIFIED PLASMA RECOVERY PROGRAM (PRP)
- K944267 — HEAT EXCHANGER MODIFICATION FOR DUO AND OPTIMA
- K933960 — PLASMA RECOVERY PROGRAM FOR THE COBE BRAT 2 AUTOLOGOUS BLOOD SALVAGE SYSTEM
- K933625 — BRAT 2 AUTOLOGUS BLOOD SALVAGE SYSTEM
- K926467 — COBE CMS-FS MEMBRANE OXYGENATOR
- K921343 — COBE PATIENT MONITORING PRODUCTS
- K922484 — COBE SAMPLING SITE
- K920312 — NEW COBE CARDIOPLEGIA SYSTEM
- K913773 — COBE BRAT SYSTEMS WITHOUT REINFUSION PROTECTION
Data sourced from openFDA. This site is unofficial and independent of the FDA.