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FDA 510(k) Application Details - K062333
Device Classification Name
Device, Anti-Snoring
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510(K) Number
K062333
Device Name
Device, Anti-Snoring
Applicant
STEVEN LAMBERG, D.D.S
555 THIRTEEN STREET, NW
WASHINGTON, DC 20004-1109 US
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Contact
JONATHAN S KAHAN
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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
08/10/2006
Decision Date
12/14/2006
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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