SALMONELLA & SHIGELLA GROUPING SERA

SALMONELLA & SHIGELLA GROUPING SERA is an FDA 510(k)-cleared medical device (K820996) manufactured by Fisher Scientific Co., LLC. 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 2, 1982. Regulation: 8.