PARKE-DAVIS NON-WOVEN SPONGE

PARKE-DAVIS NON-WOVEN SPONGE is an FDA 510(k)-cleared medical device (K810318) manufactured by Hospital Products Co.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on February 25, 1981. Regulation: 8.