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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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DAVE TORMAN
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Regulation Number
890.5860
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Classification Product Code
IMG
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More FDA Info for this Product Code
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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