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FDA 510(k) Application Details - K132792
Device Classification Name
Container, Sharps
More FDA Info for this Device
510(K) Number
K132792
Device Name
Container, Sharps
Applicant
DANIELS SHARPSMART, INC.
12264 EL CAMINO REAL, STE #400
SAN DIEGO, CA 92130 US
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Contact
ALLISON KOMIYAMA
Other 510(k) Applications for this Contact
Regulation Number
880.5570
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Classification Product Code
MMK
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More FDA Info for this Product Code
Date Received
09/06/2013
Decision Date
01/31/2014
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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