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FDA 510(k) Application Details - K030829
Device Classification Name
Device, Vibration Threshold Measurement
More FDA Info for this Device
510(K) Number
K030829
Device Name
Device, Vibration Threshold Measurement
Applicant
XILAS MEDICAL, INC.
12665 SILICON DR.
SAN ANTONIO, TX 78249 US
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Contact
RUBEN G ZAMORANO
Other 510(k) Applications for this Contact
Regulation Number
000.0000
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Classification Product Code
LLN
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More FDA Info for this Product Code
Date Received
03/14/2003
Decision Date
12/05/2003
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
NE - Neurology
Review Advisory Committee
NE - Neurology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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