71 FR 176 pg. 53569 - General Hospital and Personal Use Devices
Type: RULEVolume: 71Number: 176Page: 53569
FR document: [FR Doc. 06-55527 Filed 9-11-06; 8:45 am]
Agency: Health and Human Services Department
Sub Agency: Food and Drug Administration
Official PDF Version: PDF Version
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
21 CFR Part 880
General Hospital and Personal Use Devices
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 Umbilical occlusion device.
(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.
[FR Doc. 06-55527 Filed 9-11-06; 8:45 am]
BILLING CODE 1505-01-D