FDA 510(k) Application Details - K945954

Device Classification Name Table, Physical Therapy, Multi Function

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510(K) Number K945954
Device Name Table, Physical Therapy, Multi Function
Applicant SPINALIGHT, INC.
320 A BELL PARK DR.
WOODSTOCK, GA US
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Contact T A COX
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Regulation Number 890.5880

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Classification Product Code JFB
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Date Received 12/06/1994
Decision Date 01/19/1995
Decision SE - Substantially Equivalent
Classification Advisory Committee NE - Neurology
Review Advisory Committee PM - Physical Medicine
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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