Cardio Flow Inc.,
Cardio Flow Inc., holds FDA 510(k) medical device clearances, first cleared 2022, most recent 2025.
Top product codes for Cardio Flow Inc.,
Recent clearances by Cardio Flow Inc.,
- K250723 — FreedomFlow Orbital Circumferential Atherectomy System (H6005/ 4Fr 3-Sphere Configuration)
- K242947 — FreedomFlow Orbital Circumferential Atherectomy System
- K233483 — FreedomFlow Orbital Circumferential Atherectomy System (H6004/5Fr 3-Sphere Configuration)
- K231538 — FreedomFlow Orbital Circumferential Atherectomy System
- K213834 — Cardio Flow Peripheral Guide Wire
Data sourced from openFDA. This site is unofficial and independent of the FDA.