Phillippine Radiant C/O U.S. Polymer Industries

Phillippine Radiant C/O U.S. Polymer Industries holds 1 FDA 510(k) medical device clearance, cleared in 1988.

Top product codes for Phillippine Radiant C/O U.S. Polymer Industries

KGO — General, Plastic Surgery1 device

Recent clearances by Phillippine Radiant C/O U.S. Polymer Industries

K880480 — DUNFORD SURGEON'S STERILE GLOVESCode KGO·1988-06-17

Data sourced from openFDA. This site is unofficial and independent of the FDA.