CDRHNew
Date: October 25, 2016
The following new items were added to the CDRH web pages on October 24, 2016. Previous CDRH New Items can be found on the CDRHNew Page.
- FDA Voice blog: FDA is working with hospitals to modernize data collection about medical devices
- Letter to Viracor-IBT Laboratories, Inc. regarding Zika Virus IgG, and Zika Virus IgG and IgM Panel
- Federal Register: Medical Devices; Ear, Nose, and Throat Devices; Classification of the Eustachian Tube Balloon Dilation System
- Federal Register: Program for Parallel Review of Medical Devices
- Public Workshop - The Role of Hospitals in Modernizing Evidence Generation for Device Evaluation: Harnessing the Digital Revolution for Surveillance, December 5, 2016
- Reporting Allegations of Regulatory Misconduct
- Class I Medical Device Recall: St. Jude Medical Recalls Implantable Cardioverter Defibrillators (ICD) and Cardiac Resynchronization Therapy Defibrillators (CRT-D) Due to Premature Battery Depletion
- Summary of December 2015 - April 2016 Hospital Inspection Information - October 24, 2016
.png)
No hay comentarios:
Publicar un comentario