Vitalog Monitoring, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Vitalog Monitoring, Inc. makes
Vitalog Monitoring, Inc. manufactures physiological monitoring devices, including multichannel physiological monitoring systems and pulse oximeters. Their products capture vital signs such as heart rate, oxygen saturation, and other physiological parameters for clinical use. Modifications of their core monitors are also part of the portfolio.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Hms-4000 Physiological Monitor, Modification Ref K914620
Regimes: 510(k) Registry: 510(k)VX4 Recording Pulse Oximeter Ref K935510
Regimes: 510(k) Registry: 510(k)Hms-5000 Ref K914085
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vitalog Monitoring, Inc. have in the registry?
The registry currently lists 4 devices for Vitalog Monitoring, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vitalog Monitoring, Inc.'s devices?
Among its 4 most recently registered devices, Vitalog Monitoring, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Vitalog Monitoring, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Vitalog Monitoring, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vitalog Monitoring, Inc. in the registry?
The most recently registered devices listed for Vitalog Monitoring, Inc. include HMS-4000 PHYSIOLOGICAL MONITOR, MODIFICATION, VX4 RECORDING PULSE OXIMETER, HMS-5000 and HMS-4000 MULTICHANNEL PHYSIO MONIT SYST, MODIFIED.