FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

M.F.S. LOW AIR LOSS PULSATING BED

K Number: K893801 · Decision Jul 25, 1989
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
56
Applicant Total
5
Review Days
64

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Basic Information

Device Name
M.F.S. LOW AIR LOSS PULSATING BED
K Number
K893801
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5170
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Medical Flotation Systems, Inc.
Date Received
May 22, 1989
Decision Date
July 25, 1989
Product Code
IOQ
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
IOQ Bed, Flotation Therapy, Powered

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Other Clearances by Medical Flotation Systems, Inc.

K Number Device Name
K890200 PNEUMATIC DORSIFLEXOR
K884907 BUMPY MEDICAL MASSAGE MAT
K884908 ULTRAFLOTATION MEDICAL WHEELCHAIR
K882607 ULTRAFLOTATION BED