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FDA 510(k) Application Details - K972061
Device Classification Name
Device, Anti-Snoring
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510(K) Number
K972061
Device Name
Device, Anti-Snoring
Applicant
W. KEITH THORNTON, D.D.S.
6131 LUTHER LANE, SUITE 208
DALLAS, TX 75225 US
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Contact
W. KEITH THORNTON
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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
06/03/1997
Decision Date
08/21/1997
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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