Keisei (USA) Co., Ltd.
Country not established
- Devices
- 2
What Keisei (USA) Co., Ltd. makes
Keisei (Usa) Co., Ltd. manufactures the LIFE ISLAND 21 and KEISEI devices, which appear to be medical imaging systems designed for diagnostic purposes, likely including ultrasound or similar modalities.
These products fall under Class I and Class II regulatory classifications in the US and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Life Island 21 Ref K925651
Regimes: 510(k) Registry: 510(k)Keisei Ref K950613
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Keisei (Usa) Co., Ltd. have in the registry?
The registry currently lists 2 devices for Keisei (Usa) Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Keisei (Usa) Co., Ltd.'s devices?
Among its 2 most recently registered devices, Keisei (Usa) Co., Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Keisei (Usa) Co., Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Keisei (Usa) Co., Ltd.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Keisei (Usa) Co., Ltd. in the registry?
The most recently registered devices listed for Keisei (Usa) Co., Ltd. include LIFE ISLAND 21 and KEISEI.