Iterative Health
Country not established
- Devices
- 2
What Iterative Health makes
Iterative Health manufactures the SKOUT system, a medical imaging device designed for high-resolution, portable ultrasound imaging. The system is intended for use in clinical settings to capture detailed images of internal structures, supporting diagnostic evaluations.
The SKOUT system is classified as a Class II medical device under FDA regulations and is authorised via the 510(k) clearance process. The company is based in the United States.
Catalogue
SKOUT system Ref K253664
Regimes: 510(k) Registry: 510(k)SKOUT system Ref K251126
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Iterative Health have in the registry?
The registry currently lists 2 devices for Iterative Health. Devices recorded under merged duplicate company entries are counted once.
Which registries list Iterative Health's devices?
Among its 2 most recently registered devices, Iterative Health has devices listed in FDA 510(k) (2 devices).
What risk classes do Iterative Health's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Iterative Health's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Iterative Health in the registry?
The most recently registered devices listed for Iterative Health include SKOUT system.