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FDA 510(k) Applications Submitted by Patrick Stimart
FDA 510(k) Number
Submission Date
Device Name
Applicant
K171080
04/11/2017
ALP IFCC Gen.2
Roche Diagnostics Operations (RDO)
K161817
07/01/2016
Tina-quant Cystatin C Gen.2
Roche Diagnostics Operations (RDO)
K141925
07/16/2014
TOTAL PROTEIN URINE/CSF GEN.3
Roche Diagnostics Operations (RDO)
K113072
10/17/2011
TINA-QUANT ALBUMIN GEN.2
ROCHE DIAGNOSTICS OPERATIONS
K102016
07/19/2010
PRECICONTROL CLINCHEM MULTI 1 AND 2
Roche Diagnostics
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