Nu Tech Medical Systems
Country not established
- Devices
- 2
What Nu Tech Medical Systems makes
Nu Tech Medical Systems manufactures a butterfly needle assembly for vascular access and an infusion pump for controlled fluid delivery, including medications and nutrients.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
Butterfly Needle Assembly Ref K812404
Regimes: 510(k) Registry: 510(k)Infusion Pump Ref K812499
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nu Tech Medical Systems have in the registry?
The registry currently lists 2 devices for Nu Tech Medical Systems. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nu Tech Medical Systems's devices?
Among its 2 most recently registered devices, Nu Tech Medical Systems has devices listed in FDA 510(k) (2 devices).
What risk classes do Nu Tech Medical Systems's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Nu Tech Medical Systems's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nu Tech Medical Systems in the registry?
The most recently registered devices listed for Nu Tech Medical Systems include BUTTERFLY NEEDLE ASSEMBLY and INFUSION PUMP.