Vivometrics, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 3
What Vivometrics, Inc. makes
Vivometrics, Inc. makes wearable physiological monitoring systems, including the LifeShirt real-time system with VivoMonitor software, the LifeShirt system with VivoLogic analysis software, and a reusable multiple-patient LifeShirt with VivoLogic analysis software.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Lifeshirt Real-Time With Vivomonitor Software Ref K043604
510(k) 510(k)- 510(k) 510(k)
- 510(k) 510(k)
Frequently asked questions
How many devices does Vivometrics, Inc. have in the registry?
The registry currently lists 3 devices for Vivometrics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vivometrics, Inc.'s devices?
Among its 3 most recently registered devices, Vivometrics, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Vivometrics, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Vivometrics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vivometrics, Inc. in the registry?
The most recently registered devices listed for Vivometrics, Inc. include LIFESHIRT REAL-TIME WITH VIVOMONITOR SOFTWARE, LIFESHIRT SYSTEM WITH VIVOLOGIC ANALYSIS SOFTWARE and REUSABLE MULTIPLE-PATIENT LIFESHIRT WITH VIVOLOGIC ANALYSIS SOFTWARE.