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FDA 510(k) Application Details - K203462
Device Classification Name
Device, Anti-Snoring
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510(K) Number
K203462
Device Name
Device, Anti-Snoring
Applicant
DaSoft Partners
4079 Governor Drive #111
San Diego, CA 92122 US
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Contact
Dante Togliatti
Other 510(k) Applications for this Contact
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
11/24/2020
Decision Date
02/19/2021
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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