BECKMAN ANTISTREPTOLYSIN O, MODIFICATION

BECKMAN ANTISTREPTOLYSIN O, MODIFICATION is an FDA 510(k)-cleared medical device (K915053) manufactured by Beckman Instruments, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on March 18, 1992. Regulation: 8.