Intromed
Country not established
- Devices
- 2
What Intromed makes
Intromed manufactures PTFE peel-away microintroducers, designed for guiding catheters and guidewires in vascular and interventional procedures.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
M.I.P. - Pump Ref K882249
Regimes: 510(k) Registry: 510(k)Ptfe Peel Away Microintroducer Ref K072130
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Intromed have in the registry?
The registry currently lists 2 devices for Intromed. Devices recorded under merged duplicate company entries are counted once.
Which registries list Intromed's devices?
Among its 2 most recently registered devices, Intromed has devices listed in FDA 510(k) (2 devices).
What risk classes do Intromed's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Intromed's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Intromed in the registry?
The most recently registered devices listed for Intromed include M.I.P. - PUMP and PTFE PEEL AWAY MICROINTRODUCER.