All fees collected by the department pursuant to requests to conduct a voluntary medical device review shall be deposited into the Export Document Program Fund and, upon appropriation, shall be expended for the purpose of determining if the device is a new device or is substantially equivalent to a current or previously marked device.
(Added by Stats. 1997, Ch. 294, Sec. 12. Effective August 18, 1997.)
Last modified: October 25, 2018