MODIFICATION TO PLAYTEX TAMPONS #24002

MODIFICATION TO PLAYTEX TAMPONS #24002 is an FDA 510(k)-cleared medical device (K022882) manufactured by Playtex Products, Inc.. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 15, 2002. Regulation: 8.