
Titronics Research & Development Co.
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TYTRON C-500IR CLINICAL INFRARED IMAGING SYSTEM is an FDA 510(k)-cleared medical device (K032471) manufactured by Titronics Research & Development Co.. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on October 9, 2003. Regulation: 8.

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