Lifeclinic International, Inc.
Country not established
- Devices
- 1
What Lifeclinic International, Inc. makes
Lifeclinic International, Inc. manufactures blood pressure monitoring devices, including the LifeClinic Model 2400, which is designed for home use to measure and track systolic and diastolic blood pressure readings.
The company’s portfolio is regulated under FDA Class II devices, with products authorised via the 510(k) clearance pathway. These devices are listed in the FDA’s 510(k) registry and are intended for commercial distribution in the United States.
Catalogue
Lifeclinic, Model 2400 Ref K040562
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lifeclinic International, Inc. have in the registry?
The registry currently lists 1 device for Lifeclinic International, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lifeclinic International, Inc.'s devices?
Among its 1 most recently registered device, Lifeclinic International, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Lifeclinic International, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Lifeclinic International, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lifeclinic International, Inc. in the registry?
The most recently registered devices listed for Lifeclinic International, Inc. include LIFECLINIC, MODEL 2400.