§ 110241
54 words·~1 min read·
/ca/health-and-safety-code/110241A research copy — for the controlling text, always check the official state or federal source. Not legal advice.
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.