Bed, Patient Rotation, Powered
FDA product code IKZ · 17 cleared devices
Class 2
Physical Medicine
- Regulation
- 21 CFR 890.5225
- Review panel
- PM
- Implant
- No
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 1981-02-04 – 1998-02-20
IKZ
1998-02-20
IKZ
1998-02-02
RUMORS DYNAMIC AIR THERAPY UNIT
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IKZ
1997-04-30
CLINIDYNE ROTATIONAL THERAPY MATTRESS SYSTEM
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IKZ
1996-04-01
THE FREEDOM BED
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IKZ
1995-05-30
PULMONEX DYNAMIC AIR THERAPY UNIT
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IKZ
1995-05-16
MODEL TURN Q PLUS AUTOMATIC TURNING MATTRESS WITH LOW AIR LOSS THERAPY
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IKZ
1994-10-03
THE CRADLE
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IKZ
1993-03-22
OSCILLAIR 3000 LOW AIR LOSS KINETIC THERAPY BED
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IKZ
1992-09-09
TURN EZ BED DEVICE
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IKZ
1991-01-08
KUDO (POWERED ROTATION BED)
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IKZ
1990-11-26
ROTO REST; TRAUMA AND INTENSIVE CARE BED
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IKZ
1987-10-15
KEANE MOBILITY BED
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IKZ
1984-07-20
EMERSON MOTION BED 6-MS & 6-ME
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IKZ
1984-01-30
EGERTON TURNING & TILTING BED
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IKZ
1982-12-03
KINETIC MOTION BED
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IKZ
1982-10-22
ROTO REST KINETIC TREATMENT TABLE PEDIA
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IKZ
1981-02-04
POWERED PATIENT SYSTEM
View details →No matching devices.
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