Stericap Systems
Country not established
- Devices
- 2
What Stericap Systems makes
Stericap Systems manufactures sterile stopcock valves and associated replacement trays designed for use in intravenous (IV) fluid administration systems. These devices are intended to control fluid flow and prevent contamination during medical procedures.
The company’s products are regulated as Class II medical devices under FDA requirements, with individual devices authorised via the 510(k) clearance process. The portfolio is listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.
Catalogue
Stericap Stopcock Ref K872066
Regimes: 510(k) Registry: 510(k)Stericap Assembly And Replacement Tray Ref K872067
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Stericap Systems have in the registry?
The registry currently lists 2 devices for Stericap Systems. Devices recorded under merged duplicate company entries are counted once.
Which registries list Stericap Systems's devices?
Among its 2 most recently registered devices, Stericap Systems has devices listed in FDA 510(k) (2 devices).
What risk classes do Stericap Systems's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Stericap Systems's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Stericap Systems in the registry?
The most recently registered devices listed for Stericap Systems include STERICAP STOPCOCK and STERICAP ASSEMBLY AND REPLACEMENT TRAY.