Stuart Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Stuart Medical, Inc. makes
Stuart Medical, Inc. manufactures the Meditech Euroscaner M250, a diagnostic imaging device, and the SMI Model 210 Ambulatory ECG Monitoring System, used for continuous heart rhythm recording outside clinical settings.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Meditech Euroscanner M250 Ref K850027
Regimes: 510(k) Registry: 510(k)Smi Model 210 Ambulatory Ecg Monitoring System Ref K920294
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Stuart Medical, Inc. have in the registry?
The registry currently lists 2 devices for Stuart Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Stuart Medical, Inc.'s devices?
Among its 2 most recently registered devices, Stuart Medical, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Stuart Medical, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Stuart Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Stuart Medical, Inc. in the registry?
The most recently registered devices listed for Stuart Medical, Inc. include MEDITECH EUROSCANNER M250 and SMI MODEL 210 AMBULATORY ECG MONITORING SYSTEM.