
In-Line Diagnostics Corp.
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CRIT-LINE HEMATOCRIT ALERT (MODIFICATION) is an FDA 510(k)-cleared medical device (K953875) 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 July 22, 1996. Regulation: 8.