Insitu Systems
Country not established
- Devices
- 1
What Insitu Systems makes
Insitu Systems manufactures the Manipuseal, a medical device designed for securing and stabilizing intravenous (IV) lines and other tubular connections in clinical settings. The product is intended to reduce disconnections and improve patient safety by providing a secure, reusable connection system for medical tubing.
The Manipuseal is classified as a Class II device under FDA regulations and requires 510(k) clearance for market authorisation. The company is based in the United States.
Catalogue
Manipuseal Ref K051160
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Insitu Systems have in the registry?
The registry currently lists 1 device for Insitu Systems. Devices recorded under merged duplicate company entries are counted once.
Which registries list Insitu Systems's devices?
Among its 1 most recently registered device, Insitu Systems has devices listed in FDA 510(k) (1 device).
What risk classes do Insitu Systems's devices fall under?
Among its 1 most recently registered device, the classes recorded for Insitu Systems's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Insitu Systems in the registry?
The most recently registered devices listed for Insitu Systems include MANIPUSEAL.