Monitor, Bed Patient
FDA product code KMI · 30 cleared devices
Class 1
General Hospital
- Regulation
- 21 CFR 880.2400
- Review panel
- HO
- Implant
- No
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 1977-07-14 – 2013-10-08
KMI
2013-10-08
KMI
2013-08-15
DYNASENSE SYSTEM
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KMI
2010-07-15
VIVATRAK
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KMI
2009-04-24
MOBILECARE MONITOR, MODEL 2100
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KMI
1994-12-23
ULTIMAT-SENSOR FOR BED OCCUPANCY MONITOR
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KMI
1994-11-02
INFORMER PLUS
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KMI
1994-09-22
PM-PAGER
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KMI
1994-04-29
HOME AMB-ALERT
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KMI
1994-04-14
TELETOM
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KMI
1993-06-24
SENIOR TECH TABS 88 TRANS RA1/WRA1/R1 ANN TYPE CR1
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KMI
1993-06-16
WANDER CARE
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KMI
1992-05-14
POSEY SITTER
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KMI
1992-04-13
BARTRONIX IN-BED ACTIVITY MONITOR
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KMI
1991-09-13
AMB-ALERT
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KMI
1991-04-01
RSVP RF-2000
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KMI
1991-02-12
EXIT ALARM
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KMI
1990-09-12
ALERT BED ALARM SYSTEM
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KMI
1990-08-30
THE MONITOR ELECTRONIC BED ALARM SYSTEM
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KMI
1988-10-25
PMD SYSTEM-20
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KMI
1987-12-08
JDM SP2 SENSOR
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KMI
1987-08-06
STA-PUT
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KMI
1987-05-26
BED PATIENT PRESENCE MONITOR
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KMI
1987-01-21
RSVP SYSTEMS, SERIES I, BED-PATIENT MONITOR
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KMI
1986-04-17
THE CELL CARE SYSTEM
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KMI
1986-03-25
BED PATIENT MONITOR
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KMI
1984-07-03
FALL-SAFE VEST
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KMI
1984-07-03
FALL-SAFE MONITOR
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KMI
1984-05-07
AMBULARM
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KMI
1983-04-18
BED-CHECK: II-IFAC
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KMI
1977-07-14
MONITOR, BED, TECHNOLICS
View details →No matching devices.
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