VARICELLA-ZOSTER FA LABELLED (8-321 RF)

VARICELLA-ZOSTER FA LABELLED (8-321 RF) is an FDA 510(k)-cleared medical device (K770806) manufactured by Flow Laboratories, 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 May 19, 1977. Regulation: 8.