Pneumacare Limited
United KingdomFDA applicant, unverified
- Devices
- 1
What Pneumacare Limited makes
Pneumacare Limited manufactures the Thora-3Di (Model T-01), a medical device designed for three-dimensional imaging of thoracic anatomy, likely used in diagnostic or surgical planning applications.
The device falls under FDA Class II regulation and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Thora-3Di, Model T-01 Ref K151940
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pneumacare Limited have in the registry?
The registry currently lists 1 device for Pneumacare Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pneumacare Limited's devices?
Among its 1 most recently registered device, Pneumacare Limited has devices listed in FDA 510(k) (1 device).
What risk classes do Pneumacare Limited's devices fall under?
Among its 1 most recently registered device, the classes recorded for Pneumacare Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pneumacare Limited in the registry?
The most recently registered devices listed for Pneumacare Limited include Thora-3Di, Model T-01.