VIRGO IPA FOR DETECTION OF GENTAMICIN

VIRGO IPA FOR DETECTION OF GENTAMICIN is an FDA 510(k)-cleared medical device (K811744) manufactured by Electro-Nucleonics Laboratories, Inc.. This device is classified under the Clinical Toxicology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 9, 1981. Regulation: 8.