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FDA 510(k) Application Details - K994175
Device Classification Name
Motor, Drill, Pneumatic
More FDA Info for this Device
510(K) Number
K994175
Device Name
Motor, Drill, Pneumatic
Applicant
SODEM SYSTEMS
110 CH. DU PONT DU CENTENAIRE
GENEVA CH-1228 CH
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Contact
DANIEL BACCINO
Other 510(k) Applications for this Contact
Regulation Number
882.4370
More FDA Info for this Regulation Number
Classification Product Code
HBB
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More FDA Info for this Product Code
Date Received
12/10/1999
Decision Date
12/21/1999
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
NE - Neurology
Review Advisory Committee
NE - Neurology
Statement / Summary / Purged Status
Statement
Type
Special
Reviewed By Third Party
N
Expedited Review
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