PROBE RETRACTOR, PART #S-2L8-6

PROBE RETRACTOR, PART #S-2L8-6 is an FDA 510(k)-cleared medical device (K770414) manufactured by Acme United Corp.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 14, 1977. Regulation: 8.