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

EMERSON MOTION BED 6-MS & 6-ME

K Number: K842604 · Decision Jul 20, 1984
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
16
Applicant Total
25
Review Days
15

Basic Information

Device Name
EMERSON MOTION BED 6-MS & 6-ME
K Number
K842604
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5225
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
J. H. EMERSON CO.
Date Received
July 5, 1984
Decision Date
July 20, 1984
Product Code
IKZ
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
IKZ Bed, Patient Rotation, Powered

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