Pulseflow Technologies
United KingdomFDA applicant, unverified
- Devices
- 1
What Pulseflow Technologies makes
Pulseflow Technologies manufactures the PulseFlowDF, a device designed for the controlled delivery of pulmonary vasodilators in neonatal and pediatric patients, particularly for the management of pulmonary hypertension.
The PulseFlowDF is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
PulseFlowDF Ref K150806
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pulseflow Technologies have in the registry?
The registry currently lists 1 device for Pulseflow Technologies. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pulseflow Technologies's devices?
Among its 1 most recently registered device, Pulseflow Technologies has devices listed in FDA 510(k) (1 device).
What risk classes do Pulseflow Technologies's devices fall under?
Among its 1 most recently registered device, the classes recorded for Pulseflow Technologies's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pulseflow Technologies in the registry?
The most recently registered devices listed for Pulseflow Technologies include PulseFlowDF.