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FDA 510(k) Application Details - K031116
Device Classification Name
Diathermy, Ultrasonic, For Use In Applying Therapeutic Deep Heat
More FDA Info for this Device
510(K) Number
K031116
Device Name
Diathermy, Ultrasonic, For Use In Applying Therapeutic Deep Heat
Applicant
CHATTANOOGA GROUP
4717 ADAMS RD.
P.O. BOX 489
HIXSON, TN 37343 US
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Contact
MICK DAVIS
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Regulation Number
890.5300
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Classification Product Code
IMI
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More FDA Info for this Product Code
Date Received
04/08/2003
Decision Date
12/03/2003
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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