Infusion Systems Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Infusion Systems Corp. makes
Infusion Systems Corp. manufactures infusion devices, specifically the TEAMMATE and INTERMATE product lines.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) database. The company is based in the United States.
Catalogue
Teammate(Tm) Ref K880569
Regimes: 510(k) Registry: 510(k)Intermate(Tm) Ref K870242
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Infusion Systems Corp. have in the registry?
The registry currently lists 2 devices for Infusion Systems Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Infusion Systems Corp.'s devices?
Among its 2 most recently registered devices, Infusion Systems Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Infusion Systems Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Infusion Systems Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Infusion Systems Corp. in the registry?
The most recently registered devices listed for Infusion Systems Corp. include TEAMMATE(TM) and INTERMATE(TM).