Nuclear Pacific, Inc.
Country not established
- Devices
- 1
What Nuclear Pacific, Inc. makes
Nuclear Pacific, Inc. manufactures the Capillary Perfusion Monitor (LD5000), a device designed to measure and monitor microcirculatory blood flow in tissue, often used in critical care and surgical settings to assess perfusion levels.
The Capillary Perfusion Monitor (LD5000) is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Capillary Perfusion Monitor #LD5000 Ref K812005
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nuclear Pacific, Inc. have in the registry?
The registry currently lists 1 device for Nuclear Pacific, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nuclear Pacific, Inc.'s devices?
Among its 1 most recently registered device, Nuclear Pacific, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Nuclear Pacific, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Nuclear Pacific, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nuclear Pacific, Inc. in the registry?
The most recently registered devices listed for Nuclear Pacific, Inc. include CAPILLARY PERFUSION MONITOR #LD5000.