Fluidsense Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Fluidsense Corp. makes
Fluidsense Corp. manufactures fluid delivery systems designed for precise and controlled administration of liquids in medical settings. The FLUIDSENSE FLUID DELIVERY SYSTEM and its Model FS-01 are engineered to ensure accurate dosing and monitoring of fluid flow, supporting applications in clinical environments.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. Fluidsense Corp. is based in the United States.
Catalogue
Fluidsense Fluid Delivery System Ref K982170
Regimes: 510(k) Registry: 510(k)Fluidsense Fluid Delivery System Model Fs-01 Ref K003582
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Fluidsense Corp. have in the registry?
The registry currently lists 2 devices for Fluidsense Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fluidsense Corp.'s devices?
Among its 2 most recently registered devices, Fluidsense Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Fluidsense Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Fluidsense Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Fluidsense Corp. in the registry?
The most recently registered devices listed for Fluidsense Corp. include FLUIDSENSE FLUID DELIVERY SYSTEM and FLUIDSENSE FLUID DELIVERY SYSTEM MODEL FS-01.