FDA 510(k) Application Details - K961261

Device Classification Name Interferential Current Therapy

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510(K) Number K961261
Device Name Interferential Current Therapy
Applicant DYNATRONICS CORP.
7030 PARK CENTRE DR.
SALT LAKE CITY, UT 84121 US
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Contact JOHN S RAMEY
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Regulation Number 000.0000

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Classification Product Code LIH
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Date Received 04/02/1996
Decision Date 09/05/1996
Decision SESE - SUBST EQUIV
Classification Advisory Committee NE - Neurology
Review Advisory Committee NE - Neurology
Statement / Summary / Purged Status Statement
Type Traditional
Reviewed By Third Party N
Expedited Review



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