SEROIDEN STREPTO KIT 'EIKEN'

SEROIDEN STREPTO KIT 'EIKEN' is an FDA 510(k)-cleared medical device (K861098) manufactured by Syn-Kit, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 11, 1986. Regulation: 8.