
In-Line Diagnostics Corp.
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MODIFICATION OF CRIT-LINE MONITOR III (CLM III) is an FDA 510(k)-cleared medical device (K982412) manufactured by In-Line Diagnostics Corp.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 8, 1998. Regulation: 8.