Pako Corp.
Country not established
- Devices
- 1
What Pako Corp. makes
Pako Corp. manufactures the PAKOSTAT II, a medical device designed for monitoring and managing blood pressure in clinical settings, including intraoperative and critical care environments.
The PAKOSTAT II is classified as a Class II device under FDA regulations and is listed via the 510(k) clearance process. The company is based in the United States.
Catalogue
Pakostat Ii Ref K760846
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pako Corp. have in the registry?
The registry currently lists 1 device for Pako Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pako Corp.'s devices?
Among its 1 most recently registered device, Pako Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Pako Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Pako Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pako Corp. in the registry?
The most recently registered devices listed for Pako Corp. include PAKOSTAT II.