FDA 510(k) Application Details - K020119

Device Classification Name Stimulator, Ultrasound And Muscle, For Use In Applying Therapeutic Deep Heat

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510(K) Number K020119
Device Name Stimulator, Ultrasound And Muscle, For Use In Applying Therapeutic Deep Heat
Applicant METRON MEDICAL AUSTRALIA PTY LTD
57 ASTER AVE.
CARRUM DOWNS, VICTORIA 3201 AU
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Contact DAVE TORMAN
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Regulation Number 890.5860

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Classification Product Code IMG
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Date Received 01/14/2002
Decision Date 07/22/2002
Decision SESE - SUBST EQUIV
Classification Advisory Committee PM - Physical Medicine
Review Advisory Committee PM - Physical Medicine
Statement / Summary / Purged Status Statement
Type Traditional
Reviewed By Third Party N
Expedited Review



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