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FDA 510(k) Application Details - K132933
Device Classification Name
Device, Anti-Snoring
More FDA Info for this Device
510(K) Number
K132933
Device Name
Device, Anti-Snoring
Applicant
ALLEN J. MOSES, DDS, LTD.
233 S. WACKER DR.
CHICAGO, IL 60606 US
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Contact
ALLEN J MOSES, DDS
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Regulation Number
872.5570
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Classification Product Code
LRK
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More FDA Info for this Product Code
Date Received
09/18/2013
Decision Date
04/25/2014
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
DE - Dental
Review Advisory Committee
DE - Dental
Statement / Summary / Purged Status
Statement
Type
Special
Reviewed By Third Party
N
Expedited Review
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