{"data":{"id":"us-ca/hsc-110241","jurisdiction":"us-ca","citation":"HSC § 110241","heading":"","body":"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.","path":["Health and Safety Code - HSC","DIVISION 104. ENVIRONMENTAL HEALTH [106500. - 119406.]","PART 5. SHERMAN FOOD, DRUG, AND COSMETIC LAWS [109875. - 111929.5.]","CHAPTER 2. Administration [110045. - 110243.]","ARTICLE 4. Export Documents [110190. - 110241.]"],"source_url":"https://downloads.leginfo.legislature.ca.gov/pubinfo_2025.zip","current_through":"2026-09-13","vintage":"","retrieved_at":"2026-09-14T05:56:33Z","sha256":"4c0b57ed088545d310b013eff05fb0ec56991ba636cd946da4f3d7fff10d2313","source_id":"us-ca","stale":false,"prev":"us-ca/hsc-110240","next":"us-ca/hsc-110242"},"notice":"GroundRules: Original legal text. Not legal advice."}