KWIK KOLD PERI COLD PACK (CATALOG NUMBER TBD)

KWIK KOLD PERI COLD PACK (CATALOG NUMBER TBD) is an FDA 510(k)-cleared medical device (K970399) manufactured by Allegiance Healthcare Corp.. This device is classified under the Physical Medicine specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 2, 1997. Regulation: 8.