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FDA 510(k) Application Details - K112205
Device Classification Name
Device, Anti-Snoring
More FDA Info for this Device
510(K) Number
K112205
Device Name
Device, Anti-Snoring
Applicant
CONSUMER HEALTH PRODUCTS, INC
49 COASTAL OAK
ALISO VIEJO, CA 92656 US
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Contact
GARY MOCNIK
Other 510(k) Applications for this Contact
Regulation Number
872.5570
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Classification Product Code
LRK
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
08/01/2011
Decision Date
11/16/2011
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
DE - Dental
Review Advisory Committee
DE - Dental
Statement / Summary / Purged Status
Summary
Type
Abbreviated
Reviewed By Third Party
N
Expedited Review
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