RESP. PANEL 1 INDIRECT IMMUNOFLUORESCENCE ASSAY

RESP. PANEL 1 INDIRECT IMMUNOFLUORESCENCE ASSAY is an FDA 510(k)-cleared medical device (K922801) manufactured by Light Diagnostics. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 5, 1993. Regulation: 8.