Cobe Cardiovascular, Inc.
Cobe Cardiovascular, Inc. holds FDA 510(k) medical device clearances, first cleared 1992, most recent 2005.
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.