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FDA 510(k) Application Details - K991449
Device Classification Name
Device, Anti-Snoring
More FDA Info for this Device
510(K) Number
K991449
Device Name
Device, Anti-Snoring
Applicant
DENTAL IMAGINEERS, LLC.
804 WEST PARK AVE.
OCEAN, NJ 07712 US
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Contact
WILLIAM BELFER
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
04/26/1999
Decision Date
07/22/1999
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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