ZipThaw submitted to FDA

ZipThaw submitted to FDA

ZipThaw202 will be the first to market next generation technology blood and tissue products warming device and disposable.

The prototype devices tested at the New York Blood Center are being engineered for manufacturing. FreMon Scientific has filed form 510(K) with the FDA. As a Class II Predicate device approval could be as soon as October/November 2018. ZipThaw and ZipSleeve will be on the market within weeks of approval in all countries where FDA certification is required.