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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