
Neoprobe Corp.
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NEOPROBE 1000 GEN 1C PORTABLE RADIOISOTOPE DETECTOR & ACCESSORIES is an FDA 510(k)-cleared medical device (K962319) manufactured by Neoprobe Corp.. This device is classified under the Radiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 12, 1996. Regulation: 8.

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