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FDA 510(k) Application Details - K982321
Device Classification Name
Stimulator, Nerve, Transcutaneous, For Pain Relief
More FDA Info for this Device
510(K) Number
K982321
Device Name
Stimulator, Nerve, Transcutaneous, For Pain Relief
Applicant
CHATTANOOGA GROUP, INC.
4717 ADAMS RD.
P.O. BOX 4287
HIXSON, TN 37343 US
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Contact
CHERYL G DYER
Other 510(k) Applications for this Contact
Regulation Number
882.5890
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Classification Product Code
GZJ
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More FDA Info for this Product Code
Date Received
07/02/1998
Decision Date
02/01/1999
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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