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FDA 510(k) Application Details - K023836
Device Classification Name
Device, Anti-Snoring
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510(K) Number
K023836
Device Name
Device, Anti-Snoring
Applicant
STRONG DENTAL INC.
21525 RIDGETOP CIRCLE
SUITE 320
STERLING, VA 20166 US
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Contact
CLYDE A TAKEGUCHI
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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
11/18/2002
Decision Date
07/08/2003
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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