Starto Medical Corp.
Country not established
- Devices
- 1
What Starto Medical Corp. makes
Starto Medical Corp. manufactures the STRATO LIFEPORT Large Bore Infusion Set, a device designed for high-volume intravenous fluid administration in medical settings.
The company’s portfolio is regulated under FDA 510(k) clearance as a Class II medical device and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Strato Lifeport Large Bore Infusion Set Ref K921576
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Starto Medical Corp. have in the registry?
The registry currently lists 1 device for Starto Medical Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Starto Medical Corp.'s devices?
Among its 1 most recently registered device, Starto Medical Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Starto Medical Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Starto Medical Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Starto Medical Corp. in the registry?
The most recently registered devices listed for Starto Medical Corp. include STRATO LIFEPORT LARGE BORE INFUSION SET.