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FDA 510(k) Application Details - K953456
Device Classification Name
Exerciser, Powered
More FDA Info for this Device
510(K) Number
K953456
Device Name
Exerciser, Powered
Applicant
FLUID MOTION BIOTECHNOLOGIES, INC.
55 NORTHER BLVD.
SUITE 410
GREAT NECK, NY 11021 US
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Contact
SUSAN D GOLDSTEIN-FALK
Other 510(k) Applications for this Contact
Regulation Number
890.5380
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Classification Product Code
BXB
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More FDA Info for this Product Code
Date Received
07/19/1995
Decision Date
01/26/1996
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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