Code of Federal Regulations > Title 21 > Chapter I > Part 607 - PART 607—ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS AND LICENSED DEVICES

U.S. Code of Federal Regulations

Regulations most recently checked for updates: Aug 28, 2025

Subpart A [§ 607.1 - § 607.7] - Subpart A—General Provisions

Subpart B [§ 607.20 - § 607.39] - Subpart B—Procedures for Domestic Blood Product Establishments

Subpart C [§ 607.40 - § 607.40] - Subpart C—Procedures for Foreign Blood Product Establishments

Subpart D [§ 607.65 - § 607.65] - Subpart D—Exemptions

Subpart E [§ 607.80 - § 607.80] - Subpart E—Establishment Registration and Product Listing Of Licensed Devices