FDA 510(k) Applications for Medical Device Product Code "GOI"
(Antiserum, Fluorescent, Rabies Virus)

FDA 510(k) Number Applicant Device Name Decision Date
K972975 LIGHT DIAGNOSTICS LIGHT DIAGNOSTICS RABIES DFA REAGENT 12/22/1998


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