Flexicare
United KingdomFDA applicant, unverified
- Devices
- 1
What Flexicare makes
Flexicare manufactures CO₂ monitoring lines, including models equipped with integrated filters. These devices are designed for real-time respiratory gas analysis, typically used in critical care and anesthesia settings to measure exhaled carbon dioxide levels.
The company’s portfolio is regulated under FDA 510(k) clearance as Class II devices. These products are listed in the FDA’s 510(k) database and are based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Flexicare have in the registry?
The registry currently lists 1 device for Flexicare. Devices recorded under merged duplicate company entries are counted once.
Which registries list Flexicare's devices?
Among its 1 most recently registered device, Flexicare has devices listed in FDA 510(k) (1 device).
What risk classes do Flexicare's devices fall under?
Among its 1 most recently registered device, the classes recorded for Flexicare's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Flexicare in the registry?
The most recently registered devices listed for Flexicare include CO2 MONITORING LINE, CO2 MONITORING LINE WITH FILTER.