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FDA 510(k) Application Details - K970363
Device Classification Name
Bed, Flotation Therapy, Powered
More FDA Info for this Device
510(K) Number
K970363
Device Name
Bed, Flotation Therapy, Powered
Applicant
APEX METAL, INC.
3039 ROSWELL ST.
LOS ANGELES, CA 90065 US
Other 510(k) Applications for this Company
Regulation Number
890.5170
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Classification Product Code
IOQ
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
01/31/1997
Decision Date
11/17/1997
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
PM - Physical Medicine
Review Advisory Committee
PM - Physical Medicine
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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