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


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact