Plasiatek, LLC
Country not established
- Devices
- 1
What Plasiatek, LLC makes
Plasiatek, LLC manufactures the Plasiatek Actuator, a medical device designed to provide precise mechanical actuation for therapeutic or diagnostic applications.
The Actuator is classified as a Class II device and is listed in the FDA 510(k) registry. Plasiatek is based in the United States.
Catalogue
Plasiatek Actuator Ref K041917
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Plasiatek, LLC have in the registry?
The registry currently lists 1 device for Plasiatek, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Plasiatek, LLC's devices?
Among its 1 most recently registered device, Plasiatek, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Plasiatek, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Plasiatek, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Plasiatek, LLC in the registry?
The most recently registered devices listed for Plasiatek, LLC include PLASIATEK ACTUATOR.