General Hospital and Personal Use Devices
---
identifier: "/us/fr/06-55527"
source: "fr"
legal_status: "authoritative_unofficial"
title: "General Hospital and Personal Use Devices"
title_number: 0
title_name: "Federal Register"
section_number: "06-55527"
section_name: "General Hospital and Personal Use Devices"
positive_law: false
currency: "2006-09-12"
last_updated: "2006-09-12"
format_version: "1.1.0"
generator: "[email protected]"
agency: "Health and Human Services Department"
document_number: "06-55527"
document_type: "rule"
publication_date: "2006-09-12"
agencies:
- "Health and Human Services Department"
- "Food and Drug Administration"
cfr_references:
- "21 CFR Part 880"
fr_citation: "71 FR 53569"
fr_volume: 71
---
# Umbilical occlusion device.
**CFR Correction**
In Title 21 of the Code of Federal Regulations, parts 800 to 1299, revised as of April 1, 2006, on page 410, in § 880.5950, paragraph (b) is corrected to read as follows:
§ 880.5950
(b) *Classification.* Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter, subject to the limitations in § 880.9.