System, Hemodialysis, Access Recirculation Monitoring
FDA product code MQS · 18 cleared devices
Class 2
Gastroenterology, Urology
- Regulation
- 21 CFR 876.5820
- Review panel
- GU
- Implant
- No
- Life sustaining
- Yes
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 1996-06-21 – 2023-12-14
MQS
2023-12-14
MQS
2019-01-16
Dosis SAM
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MQS
2013-12-19
PHYSOFT AMS
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MQS
2004-11-08
VASC-ALERT
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MQS
2002-12-04
TRANSONIC SYRINGE WARMER, MODEL SYR-1000
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MQS
2002-08-12
TRANSONIC FLOW-QC SET MODEL ADT1010
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MQS
2000-12-20
CRIT-LINE MONITOR III (CLM III)
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MQS
2000-01-20
HP M2376A DEVICE LINK SYSTEM
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MQS
1999-07-30
CRIT-LINE MONITOR III (CLM III)
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MQS
1999-04-30
HP M2376A DEVICE LINK SYSTEM
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MQS
1998-10-09
MODIFICATION OF CRIT-LINE MONITOR III (CLM III)
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MQS
1998-10-06
TRANSONIC HEMODIALYSIS MONITOR, CARDIAC OUTPUT, MODEL HD01-CO
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MQS
1997-12-11
CRIT-LINE MONITOR (CLMIII)
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MQS
1997-02-11
HD01-SERIES TRANSONIC HEMODIALYSIS MONITOR (R%,QA,CO,QB,QB2)
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MQS
1997-02-06
COBE HEMODYNAMIC RECIRCULATION MONITOR
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MQS
1996-07-23
CRIT-LINE HEMATOCRIT ALERT (MODIFICATION)
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MQS
1996-07-03
FRESENIUS BLOOD TEMPERATURE MONITOR
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MQS
1996-06-21
KNOW-RECIRC
View details →No matching devices.
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