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FDA 510(k) Application Details - K070888
Device Classification Name
Stimulator, Muscle, Powered
More FDA Info for this Device
510(K) Number
K070888
Device Name
Stimulator, Muscle, Powered
Applicant
CEC ELECTRONICA S.R.L.
M.P. MIGAV 20187
INDUSTRIAL PARK 13
MIZPE AVIV 20187 IL
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Contact
BENNY ARAZY
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Regulation Number
890.5850
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Classification Product Code
IPF
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More FDA Info for this Product Code
Date Received
03/30/2007
Decision Date
07/03/2008
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
PM - Physical Medicine
Review Advisory Committee
PM - Physical Medicine
Statement / Summary / Purged Status
Summary
Type
Abbreviated
Reviewed By Third Party
N
Expedited Review
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