Petra Intl. Co.
Country not established
- Devices
- 1
What Petra Intl. Co. makes
Petra Intl. Co. manufactures the Pointer F-3, a medical device designed for precise anatomical marking or localization, commonly used in surgical or diagnostic procedures.
The Pointer F-3 is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Pointer F-3 Ref K833037
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Petra Intl. Co. have in the registry?
The registry currently lists 1 device for Petra Intl. Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Petra Intl. Co.'s devices?
Among its 1 most recently registered device, Petra Intl. Co. has devices listed in FDA 510(k) (1 device).
What risk classes do Petra Intl. Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Petra Intl. Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Petra Intl. Co. in the registry?
The most recently registered devices listed for Petra Intl. Co. include POINTER F-3.