US FDA grants 510(k) for CardieX's arterial health monitor
US FDA grants 510(k) for CardieX's arterial health monitor
The US Food and Drug Administration (FDA) has granted 510(k) clearance for CardieX’s CONNEQT Pulse, a new arterial health monitor.
Bob Hayes on LinkedIn: Arterial health monitor CONNEQT Pulse gains FDA 510(k) clearance
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CardieX Secures US FDA Approval for Medical Device Companion Application -May 18, 2022 at 04:24 am EDT
Masimo receives FDA 501(k) clearance for Masimo W1 smartwatch for telehealth monitoring - News
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blood pressure MobiHealthNews
FDA Grants 510(k) Clearance for the CONNEQT Pulse, a World-First Vascular Biometric Health Monitor - CONNEQT Health
