
Hyman, Phelps & McNamara, P.C.
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PROPHY PRO. is an FDA 510(k)-cleared medical device (K945834) manufactured by Hyman, Phelps & McNamara, P.C.. This device is classified under the Dental specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on February 12, 1995. Regulation: 8.