MERETEK BREATH TEST FOR H.PYLORI COLLECTION KIT

MERETEK BREATH TEST FOR H.PYLORI COLLECTION KIT is an FDA 510(k)-cleared medical device (K952220) manufactured by Meretek Diagnostics, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 16, 1996. Regulation: 8.