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FDA 510(k) Application Details - K113022
Device Classification Name
Device, Anti-Snoring
More FDA Info for this Device
510(K) Number
K113022
Device Name
Device, Anti-Snoring
Applicant
SLEEP SCIENCE PARTNERS, INC.
900 Larkspur Landing Circle
Suite 207
Larkspur, CA 94939 US
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Contact
HEATHER FLICK
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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
10/11/2011
Decision Date
06/11/2012
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
DE - Dental
Review Advisory Committee
DE - Dental
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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