FDA 510(k) Applications Submitted by ROBERT A GREGG

FDA 510(k) Number Submission Date Device Name Applicant
K022516 07/30/2002 ELECSYS PROBNP IMMUNOASSAY ROCHE DIAGNOSTICS CORP.
K033612 11/17/2003 FACTOR II (PROTHROMBIN) G20210A KIT ROCHE DIAGNOSTICS CORP.
K033734 11/28/2003 LIGHTCYCLER INSTRUMENT VERSION 1.2 ROCHE DIAGNOSTICS CORP.
DEN030005 12/08/2003 FACTOR V LEIDEN KIT ROCHE DIAGNOSTICS CORP.
K182930 10/22/2018 PerioLase Nd:YAG Pulsed Dental Laser System Millennium Dental Technologies, Inc.


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