
Chesebrough-Pond'S U.S.A. Co.
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BLISTERFILM TRANSPARENT DRESSING is an FDA 510(k)-cleared medical device (K851383) manufactured by Chesebrough-Pond'S U.S.A. Co.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 4, 1985. Regulation: 8.