---
kind: "unit"
title: "21"
title_heading: "Food and Drugs"
key: "chI/subchF/part607"
level: "part"
label: "Part 607"
heading: "Establishment Registration and Product Listing for Manufacturers of Human Blood and Blood Products and Licensed Devices"
release: "ecfr-current"
date: "2026-08-27"
url: "https://uscodex.org/cfr/21/chI-subchF-part607"
sections_count: 16
---

# Part 607 — Establishment Registration and Product Listing for Manufacturers of Human Blood and Blood Products and Licensed Devices

Title 21 C.F.R. — Food and Drugs › Chapter I — Food and Drug Administration, Department of Health and Human Services › Subchapter F — Biologics

## Contents

- [Subpart A — General Provisions](/cfr/21/chI-subchF-part607-subpartA.md)
- [Subpart B — Procedures for Domestic Blood Product Establishments](/cfr/21/chI-subchF-part607-subpartB.md)
- [Subpart C — Procedures for Foreign Blood Product Establishments](/cfr/21/chI-subchF-part607-subpartC.md)
- [Subpart D — Exemptions](/cfr/21/chI-subchF-part607-subpartD.md)
- [Subpart E — Establishment Registration and Product Listing Of Licensed Devices](/cfr/21/chI-subchF-part607-subpartE.md)