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FDA 510(k) Application Details - K973624
Device Classification Name
Bed, Flotation Therapy, Powered
More FDA Info for this Device
510(K) Number
K973624
Device Name
Bed, Flotation Therapy, Powered
Applicant
AIR MED ASSIST PRODUCTS
P.O. BOX 154 (FEDERAL BLDG.)
65 N. MAIN, STE
TOOLE, UT 84074-0154 US
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Contact
JOHN E LINCOLN
Other 510(k) Applications for this Contact
Regulation Number
890.5170
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Classification Product Code
IOQ
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More FDA Info for this Product Code
Date Received
09/23/1997
Decision Date
01/21/1998
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
PM - Physical Medicine
Review Advisory Committee
PM - Physical Medicine
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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