RESPIRACULT-STREP DEEP BED CULTURE PAD

RESPIRACULT-STREP DEEP BED CULTURE PAD is an FDA 510(k)-cleared medical device (K821659) manufactured by Orion Diagnostica, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 4, 1982. Regulation: 8.