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FDA 510(k) Application Details - K130538
Device Classification Name
More FDA Info for this Device
510(K) Number
K130538
Device Name
WINX SLEEP THERAPY SYSTEM
Applicant
APNICURE, INC.
900 CHESAPEAKE DR
REDWOOD CITY, CA 94063 US
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Contact
CHRIS DANIEL
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Regulation Number
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Classification Product Code
OZR
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Date Received
03/01/2013
Decision Date
05/22/2013
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
DE - Dental
Review Advisory Committee
AN - Anesthesiology
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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