Cpi, Inc.
Country not established
- Devices
- 1
What Cpi, Inc. makes
Cpi, Inc. manufactures the Ambulatory Insulin Infusion Pump 9205, a Class II medical device designed for continuous subcutaneous insulin delivery in diabetic patients.
This device is regulated under FDA 510(k) clearance as a Class II product and is listed in the FDA 510(k) database. The company is based in the United States.
Catalogue
Ambulatory Insulin Infusion Pump 9205 Ref K823193
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cpi, Inc. have in the registry?
The registry currently lists 1 device for Cpi, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cpi, Inc.'s devices?
Among its 1 most recently registered device, Cpi, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Cpi, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cpi, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cpi, Inc. in the registry?
The most recently registered devices listed for Cpi, Inc. include AMBULATORY INSULIN INFUSION PUMP 9205.