Light Diagnostics
Light Diagnostics holds FDA 510(k) medical device clearances, first cleared 1993, most recent 1999.
Top product codes for Light Diagnostics
Recent clearances by Light Diagnostics
- K991880 — LIGHT DIAGNOSTICS SIMULFLUOR HSV 1/2 IMMUNOFLUORECENCE ASSAY
- K990141 — LIGHT DIAGNOSTICS SIMULFLUOR HSV/VZV IMMUNOFLOURESCENCE ASSAY, MODEL 3295
- K972975 — LIGHT DIAGNOSTICS RABIES DFA REAGENT
- K974302 — LIGHT DIAGNOSTICS SIMULFLUOR FLU A/FLU B
- K951821 — CYTOMEGALOVIRUS DIRECT IMMUNOFLUORESCENCE ASSAY
- K951799 — VARICELLA-ZOSTER VIRUS DIRECT IMMUNOFLUORESCENCE ASSAY
- K940017 — POLIOVIRUS 3 MONOCLONAL ANTIBODY
- K940026 — POLIOVIRUS BLEND MONOCLONAL ANTIBODIES
- K940034 — POLIOVIRUS 2 MONOCLONAL ANTIBODY
- K936251 — COXSACKIEVIRUS B3 MONOCLONAL ANTIBODY
- K936252 — COXSACKIEVIRUS B@ MONOCLONAL ANTIBODY
- K936253 — COXSACKIEVIRUS B4 MONOCLONAL ANTIBODY
- K936254 — COCKSACKIEVIRUS B6 MONOCLONAL ANTIBODY
- K940018 — POLIOVIRUS 1 MONOCLONAL ANTIBODY
- K940363 — ENTEROVIRUS 70 MONCLONAL ANTIBODY
- K944191 — ANTI-NUCLEAR ANTIBODY(ANA) TEST KIT W/MOUSE LIVER
- K944192 — ANTI-NUCLEAR ANTIBODY (ANA) TEST KIT W/RAT LIVER
- K935809 — CYTOMEGALOVIRUS INDIRECT IMMUNOFLUORESCENCE ASSAY
- K922801 — RESP. PANEL 1 INDIRECT IMMUNOFLUORESCENCE ASSAY
Data sourced from openFDA. This site is unofficial and independent of the FDA.