BIOVALVE MINI-JECT NEEDLEFREE INJECTOR

BIOVALVE MINI-JECT NEEDLEFREE INJECTOR is an FDA 510(k)-cleared medical device (K051985) manufactured by Biovalve Technologies, Inc.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 16, 2005. Regulation: 8.