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FDA 510(k) Application Details - K960969
Device Classification Name
Stimulator, Nerve, Transcutaneous, For Pain Relief
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510(K) Number
K960969
Device Name
Stimulator, Nerve, Transcutaneous, For Pain Relief
Applicant
ZIMMER ELEKTROMEDIZIN GMBH
9 JUNKERSSTRABE
D7910 NEU-ULM DE
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Contact
DUCHESS GRANGER
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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
03/11/1996
Decision Date
05/15/1996
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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