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FDA 510(k) Application Details - K020893
Device Classification Name
Device, Anti-Snoring
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510(K) Number
K020893
Device Name
Device, Anti-Snoring
Applicant
DENNIS R. BAILEY, DDS
7901 EAST BELLEVIEW AVE.
SUITE 200
ENGLEWOOD, CO 80111 US
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Contact
DENNIS R BAILEY
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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
03/19/2002
Decision Date
05/28/2002
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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