Bed, Air Fluidized
FDA product code INX · 28 cleared devices
Class 2
Physical Medicine
- Regulation
- 21 CFR 890.5160
- Review panel
- PM
- Implant
- No
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 1976-11-24 – 1998-01-16
INX
1998-01-16
INX
1997-05-28
CLINITRON RITE-HITE
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INX
1995-02-27
CLINITRON ELEXIS
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INX
1995-02-07
CLINITRON AT HOME AIR FLUIDED THERAPY
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INX
1994-02-17
X-20 AIR SUPPORT BED
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INX
1994-02-02
LOW AIR LOSS MATTRESS, MODIFICATION
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INX
1993-10-15
DYLNAMEDICS A.S.A.P.
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INX
1993-03-24
COMFORT CARE LOW AIR LOSS THERAPY BED
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INX
1993-02-12
REM-AIR
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INX
1992-01-24
CLINITRON C-II
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INX
1991-11-22
SMITH AND DAVIS PRESSURE THERAPY SYSTEM
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INX
1991-06-06
THE MEDISCUS PEDCARE MANAGEMENT SYSTEM-MODEL 2
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INX
1991-04-05
DERMATEK 4000
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INX
1990-10-10
STAGE IV, AIR-FLUIDIZE BED
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INX
1989-02-10
SUPERCAIR
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INX
1988-12-07
TASSI MK2
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INX
1988-11-18
MICROAIR FLUIDIZED AIR BED
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INX
1988-11-14
FLUIDAIR
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INX
1988-07-13
MODEL 5000 AIR-FLUIDIZED SUPPORT SYSTEM
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INX
1988-02-16
MODIFIED AIR FLUIDIZED BED, KINAIR
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INX
1987-02-04
SKYTRON MODEL 610-2
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INX
1985-09-05
AIR PLUS AIR FLUIDIZED THERAPY SYSTEMS
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INX
1984-09-05
CLINITRON AIR FLUIDIZED SUPPORT J-101UD
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INX
1984-08-02
APOLLO AIR FLUIDIZED BED
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INX
1984-01-17
MED-OPEDIC SLEEP SYSTEM
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INX
1982-01-12
CLINITRON AIR FLUIDIZED SUPPORT SYSTEM
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INX
1981-03-06
NEO-WAVE SYSTEM
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INX
1976-11-24
MEDISCUS AIR BED
View details →No matching devices.
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