StacksVerified U.S. regulatory reference

21 CFR §801.122

Verified against eCFR.gov as of June 20, 2026View official text on eCFR.gov
A device intended for processing, repacking, or use in the manufacture of another drug or device shall be exempt from section 502(f)(1) of the act if its label bears the statement “Caution: For manufacturing, processing, or repacking”.