Accustat, Inc.
Country not established
- Devices
- 1
What Accustat, Inc. makes
Accustat, Inc. manufactures the Accustat Model 102, a non-invasive blood monitoring device designed for continuous or intermittent measurement of key blood parameters without requiring venipuncture or arterial puncture.
The company’s portfolio is regulated under FDA’s Class II device classification and requires 510(k) clearance. The device is listed in the FDA’s 510(k) premarket notification database. The manufacturer is based in the United States.
Catalogue
Accustat Model 102 Non-Invasive Blood Monitoring Ref K881272
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Accustat, Inc. have in the registry?
The registry currently lists 1 device for Accustat, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Accustat, Inc.'s devices?
Among its 1 most recently registered device, Accustat, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Accustat, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Accustat, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Accustat, Inc. in the registry?
The most recently registered devices listed for Accustat, Inc. include ACCUSTAT MODEL 102 NON-INVASIVE BLOOD MONITORING.