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FDA 510(k) Application Details - K973884
Device Classification Name
Device, Anti-Snoring
More FDA Info for this Device
510(K) Number
K973884
Device Name
Device, Anti-Snoring
Applicant
FRANTZ DESIGN, INC.
400 MEDICAL CENTER, #209
WEBSTER, TX 77598 US
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Contact
DONALD FRANTZ
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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
10/14/1997
Decision Date
01/09/1998
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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