Lifewatch Systems, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Lifewatch Systems, Inc. makes
Lifewatch Systems, Inc. manufactures continuous glucose monitoring systems, including the INFAGUARD™ for neonatal glucose tracking, the Lifewatch Sensor Belt for real-time glucose level detection, and the Lifewatch® Portable Monitoring System for ambulatory patient use.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
Infaguard Tm Ref K854705
Regimes: 510(k) Registry: 510(k)Lifewatch Sensor Belt Ref K864487
Regimes: 510(k) Registry: 510(k)Lifewatch(R) Portable Monitoring System Ref K864419
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lifewatch Systems, Inc. have in the registry?
The registry currently lists 3 devices for Lifewatch Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lifewatch Systems, Inc.'s devices?
Among its 3 most recently registered devices, Lifewatch Systems, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Lifewatch Systems, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Lifewatch Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lifewatch Systems, Inc. in the registry?
The most recently registered devices listed for Lifewatch Systems, Inc. include INFAGUARD TM, LIFEWATCH SENSOR BELT and LIFEWATCH(R) PORTABLE MONITORING SYSTEM.