Suction Control, Intracardiac, Cardiopulmonary Bypass
FDA product code DWD · 15 cleared devices
Class 2
Cardiovascular
- Regulation
- 21 CFR 870.4430
- Review panel
- CV
- Implant
- No
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 1976-12-09 – 2000-02-18
DWD
2000-02-18
DWD
1993-09-29
NIKKISO NK PUMP
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DWD
1992-01-07
B-D ULTRA-VUE PROCEDURE NEEDLE W/ WESTCOTT TYPE PT
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DWD
1992-01-07
B-D ULTRA-VUE PROCEDURE NEEDLE W/ CHIBA TYPE POINT
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DWD
1992-01-07
B-D ULTRA-VUE PROCEDURE NEEDLE W/ SPINAL TYPE PT.
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DWD
1991-01-15
DURAFLO II HEPARIN TREATED SUCTION WANDS VAR. MOD.
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DWD
1990-01-19
MEDISEAL SUCTION CANISTER
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DWD
1987-01-06
MODIFIED RLV-2100 B
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DWD
1986-11-18
SARNS SAFETY LOOP
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DWD
1986-08-29
LEFT VENTRICULAR VENT VALVE MODEL NO. GLV
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DWD
1986-06-26
SUCTION CONTROL VALVE (NONADJUSTABLE) CAT.RLV-2100
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DWD
1985-08-05
AJDJUSTABLE SUCTION CONTROL VALVE
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DWD
1983-02-28
VEINPREP VEIN GRAFT PREP. KIT A277723
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DWD
1983-02-28
IL VIDEO 22,21 & II ATOMIC SPECTROPHOTO-
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DWD
1976-12-09
VACUUM RELIEF VALVE
View details →No matching devices.
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