CDRHNew
Date: September 7, 2017
The following new items were added to the CDRH web pages on September 6, 2017. Previous items can be found on the CDRHNew Page.
- Digital Health Entrepreneur-in-Residence Program
- Class I Medical Device Recall: Datascope Corp./MAQUET Recalls Intra-Aortic Balloon Pumps Due to False Blood Detection Alarm and Ingress of Fluid into the Intra-Aortic Balloon Pump
- Federal Register: Design Considerations and Premarket Submission Recommendations for Interoperable Medical Devices; Guidance for Industry and Food and Drug Administration Staff; Availability
- FDA Voice blog: Interoperability: FDA's Final Guidance on Smart, Safe, Medical Device Interactions
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