Gp&P Co., Ltd.
Country not established
- Devices
- 1
What Gp&P Co., Ltd. makes
Gp&P Co., Ltd. manufactures the DCAS I, a device designed for diagnostic cardiovascular assessments, including intracardiac electrophysiology studies and arrhythmia mapping.
The DCAS I is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Dcas I Ref K140869
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gp&P Co., Ltd. have in the registry?
The registry currently lists 1 device for Gp&P Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gp&P Co., Ltd.'s devices?
Among its 1 most recently registered device, Gp&P Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Gp&P Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Gp&P Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Gp&P Co., Ltd. in the registry?
The most recently registered devices listed for Gp&P Co., Ltd. include DCAS I.