HYBRIWICK SYSTEM: HERPES DNA PROBE TEST KIT

HYBRIWICK SYSTEM: HERPES DNA PROBE TEST KIT is an FDA 510(k)-cleared medical device (K873529) manufactured by Diagnostic Hybrids, Inc.. This device is classified under the Microbiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 24, 1988. Regulation: 8.