Three events with the AutoPulse device were identified from searches of the US Food and Drug Administration (FDA) database: Manufacturer and User Device Facility Experience (MAUDE). One of the events ...
Air Methods Enhances Patient Care and Safety with Nationwide Deployment of Zoll® AutoPulse® NXT Provided by GlobeNewswire May 1, 2025, 2:30:52 PM ...
This briefing describes the regulated use of the technology for the indication specified, in the setting described, and with any other specific equipment referred to. It is the responsibility of ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback