P.T. Panca Pusaka Deli
Country not established
- Devices
- 1
What P.T. Panca Pusaka Deli makes
P.T. Panca Pusaka Deli manufactures the Penetrease, a medical device designed for percutaneous procedures to create controlled access pathways in tissue.
The Penetrease is classified as a Class II device under FDA regulations and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Penetrease Ref K980078
510(k) 510(k)
Frequently asked questions
How many devices does P.T. Panca Pusaka Deli have in the registry?
The registry currently lists 1 device for P.T. Panca Pusaka Deli. Devices recorded under merged duplicate company entries are counted once.
Which registries list P.T. Panca Pusaka Deli's devices?
Among its 1 most recently registered device, P.T. Panca Pusaka Deli has devices listed in FDA 510(k) (1 device).
What risk classes do P.T. Panca Pusaka Deli's devices fall under?
Among its 1 most recently registered device, the classes recorded for P.T. Panca Pusaka Deli's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from P.T. Panca Pusaka Deli in the registry?
The most recently registered devices listed for P.T. Panca Pusaka Deli include PENETREASE.