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FDA 510(k) Applications Submitted by FABIO ROTA
FDA 510(k) Number
Submission Date
Device Name
Applicant
K070971
04/06/2007
MODIFICATION TO SENTINEL CLIN CHEM CAL
SENTINEL CH. SRL
K070987
04/06/2007
SENTINEL LITHIUM ASSAY
SENTINEL CH SPA
K081533
06/02/2008
SENTINEL PLASMAPROTEINS CAL 3X
SENTINEL CH. SpA
K102706
09/20/2010
CKMB UDR ASSAY
SENTINEL CH. SpA
K073634
12/26/2007
MULTIGENT CREATININE (ENZYMATIC) ASSAY
SENTINEL CH. SpA
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