Interventional Innovations Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Interventional Innovations Corp. makes
Interventional Innovations Corp. manufactures infusion catheters, including the FLOWER INFUSION CATHETER (variants F-25/50, F-60/70) and the SEGUE INFUSION CATHETER, designed for targeted drug delivery or fluid infusion during medical procedures.
These devices are classified as Class II under US regulations and are listed via FDA 510(k) clearance. The company is based in the United States.
Catalogue
Flower Infusion Catheter Model F-25/50, F-60/70 Ref K955525
Regimes: 510(k) Registry: 510(k)Segue Infusion Catheter Ref K964154
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Interventional Innovations Corp. have in the registry?
The registry currently lists 2 devices for Interventional Innovations Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Interventional Innovations Corp.'s devices?
Among its 2 most recently registered devices, Interventional Innovations Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Interventional Innovations Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Interventional Innovations Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Interventional Innovations Corp. in the registry?
The most recently registered devices listed for Interventional Innovations Corp. include FLOWER INFUSION CATHETER MODEL F-25/50, F-60/70 and SEGUE INFUSION CATHETER.