CFR›Title 21›Chapter I›Part 230 ContainsSubparts A–CCorpusDaily eCFRDisplayed edition2026-04-15Last updated2026-04-15 PART 230—CERTIFICATION AND POSTMARKETING REPORTING FOR DESIGNATED MEDICAL GASES Subparts A Subpart A—General Provisions Sections 230.1–230.3 B Subpart B—Certification of Designated Medical Gases Sections 230.50–230.150 C Subpart C—Postmarketing Quality and Safety Reporting Sections 230.205–230.230 Authority21 U.S.C. 321, 331, 351, 352, 353, 355, 355a, 355f, 356, 356a, 356b, 356c, 356e, 360b, 360cc, 360ddd, 360ddd-1, 371, 374, 379e, 379k-1, 381.Source89 FR 51777, June 18, 2024, unless otherwise noted. Previous 226 Part 226—Current Good Manufacturing Practice for Type a Medicated Articles Next 250 Part 250—Special Requirements for Specific Human Drugs