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FDA 510(k) Application Details - K062951
Device Classification Name
Device, Anti-Snoring
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510(K) Number
K062951
Device Name
Device, Anti-Snoring
Applicant
AIRWAY MANAGEMENT INC.
6116 NORTH CENTRAL EXPRESSWAY
SUITE 605
DALLAS, TX 75206 US
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Contact
DARREN HENDERSON
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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
09/29/2006
Decision Date
12/12/2006
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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