FDA 510(k) Application Details - K032652

Device Classification Name Stimulator, Muscle, Powered

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510(K) Number K032652
Device Name Stimulator, Muscle, Powered
Applicant RS MEDICAL
14401 S.E. FIRST ST.
VANCOUVER, WA 98684 US
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Contact MICHAEL B MCGRAW
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Regulation Number 890.5850

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Classification Product Code IPF
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Date Received 08/28/2003
Decision Date 09/12/2003
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 Y
Expedited Review



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