ClearanceBrief
Company ยท US

Cardiovascular Devices, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1982 to 1989. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
DTYSensor, Blood-Gas, In-Line, Cardiopulmonary Bypass3
DRYMonitor, Blood-Gas, On-Line, Cardiopulmonary Bypass2
CBZAnalyzer, Ion, Hydrogen-Ion (Ph), Blood-Phase, Indwelling1
CCEAnalyzer, Gas, Oxygen, Partial Pressure, Blood-Phase, Indwelling1
DJYIon-Exchange Chromatography1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
May 23, 1989K890113THE CDI(R) SYSTEM 400
Cardiovascular Devices, Inc.
DJY
Jan 30, 1989K884228CDI(R) 2000 BLOOD GAS MONITOR
Cardiovascular Devices, Inc.
CBZ
Jun 5, 1987K871221CDI(TM) EXTRACORPOREAL BLOOD GAS SYSTEM 300
Cardiovascular Devices, Inc.
DRY
Feb 19, 1987K864703MODIFIED GAS-STAT(TM) MONITORING SYSTEM
Cardiovascular Devices, Inc.
DTY
Jan 10, 1985K843912INTRAVASCULAR BLOOD GAS SYSTEM
Cardiovascular Devices, Inc.
CCE
Apr 17, 1984K840749GAST STAT MONITORING SYSTEM
Cardiovascular Devices, Inc.
DTY
May 27, 1983K831225GAS-STAT MONITORING SYSTEM
Cardiovascular Devices, Inc.
DRY
Dec 22, 1982K822000EXTRACORPOREAL BLOOD GAS SYSTEM
Cardiovascular Devices, Inc.
DTY

Latest recalls

DateFirm and productCodeLinked 510(k)
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