federal_register: 2011-22107
Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API
This data as json
| document_number | title | type | abstract | publication_date | pub_year | pub_month | html_url | pdf_url | agency_names | agency_ids | excerpts |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 2011-22107 | Effective Date of Requirement for Premarket Approval for Cardiovascular Permanent Pacemaker Electrode; Correction | Proposed Rule | The Food and Drug Administration (FDA) is correcting a proposed rule that appeared in the Federal Register of August 8, 2011 (76 FR 48058). The document proposed to require the filing of a premarket approval application or a notice of completion of a product development protocol for the class III preamendments device: Cardiovascular permanent pacemaker electrode. The document was published with an incorrect Internet address for the first reference in the References section. This document corrects that error. | 2011-08-30 | 2011 | 8 | https://www.federalregister.gov/documents/2011/08/30/2011-22107/effective-date-of-requirement-for-premarket-approval-for-cardiovascular-permanent-pacemaker | https://www.govinfo.gov/content/pkg/FR-2011-08-30/pdf/2011-22107.pdf | Health and Human Services Department; Food and Drug Administration | 221,199 | The Food and Drug Administration (FDA) is correcting a proposed rule that appeared in the Federal Register of August 8, 2011 (76 FR 48058). The document proposed to require the filing of a premarket approval application or a notice of completion of a... |