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FDA 510(k) Application Details - K131087
Device Classification Name
Container, Sharps
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510(K) Number
K131087
Device Name
Container, Sharps
Applicant
REHRIG PACIFIC COMPANY
614 HUNTERS LANE
BRENTWOOD, TN 37027 US
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Contact
DAVID OLMSTEAD
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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
04/18/2013
Decision Date
07/12/2013
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Summary
Type
Abbreviated
Reviewed By Third Party
N
Expedited Review
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