Atlas FDA

KEANE MOBILITY BED

FDA 510(k) clearance K873047 · decided 1987-10-15

Clearance details

K-number
K873047
Device name
KEANE MOBILITY BED
Applicant
Surgi-Med, Inc.
Decision
Substantially Equivalent
Date received
1987-08-04
Decision date
1987-10-15
Days to decision
72 days
Clearance type
Traditional
Product code
IKZ
Device class
2
Regulation number
890.5225
Medical specialty
Physical Medicine
Advisory committee
Physical Medicine
Location
Lansing, MI, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
PRESSUREGUARD IV (K972486)Span-America Medical Systems, Inc.1998-02-20
RUMORS DYNAMIC AIR THERAPY UNIT (K972111)Hill-Rom, Inc.1998-02-02
CLINIDYNE ROTATIONAL THERAPY MATTRESS SYSTEM (K962788)Gaymar Industries, Inc.1997-04-30
THE FREEDOM BED (K954671)Probed Medical Technologies, Inc.1996-04-01
PULMONEX DYNAMIC AIR THERAPY UNIT (K950756)Hill-Rom, Inc.1995-05-30
MODEL TURN Q PLUS AUTOMATIC TURNING MATTRESS WITH LOW AIR LOSS THERAPY (K950681)Invacare Corp.1995-05-16
THE CRADLE (K933964)The Primal Energy Research Foundation1994-10-03
OSCILLAIR 3000 LOW AIR LOSS KINETIC THERAPY BED (K923710)Progressive Medical Technology, Inc.1993-03-22
TURN EZ BED DEVICE (K922473)Med-Ez, Inc.1992-09-09
KUDO (POWERED ROTATION BED) (K905390)Kinetic Concepts, Inc.1991-01-08
ROTO REST; TRAUMA AND INTENSIVE CARE BED (K905113)Ethos Medical Products , Ltd.1990-11-26
EMERSON MOTION BED 6-MS & 6-ME (K842604)J. H. Emerson Co.1984-07-20

Recalls involving this device

No recalls on record reference this clearance.