
Snowden-Pencer
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DIAMOND-TOUCH AND MICRO DIAMOND-TOUCH INSTRUMENTS/DIAMOND-LINE INSTRUMENTS/DIAMOND-PORT(ACCESS PARTS) is an FDA 510(k)-cleared medical device (K960400) manufactured by Snowden-Pencer. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on March 11, 1996. Regulation: 8.