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FDA 510(k) Application Details - K091818
Device Classification Name
Needle, Conduction, Anesthetic (W/Wo Introducer)
More FDA Info for this Device
510(K) Number
K091818
Device Name
Needle, Conduction, Anesthetic (W/Wo Introducer)
Applicant
LAURIMED LLC
500 ARGUELLO STREET, SUITE 100
REDWOOD CITY, CA 94063 US
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Contact
SEVRINA CIUCCI
Other 510(k) Applications for this Contact
Regulation Number
868.5150
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Classification Product Code
BSP
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More FDA Info for this Product Code
Date Received
06/18/2009
Decision Date
09/23/2009
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
AN - Anesthesiology
Review Advisory Committee
AN - Anesthesiology
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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