Cro, LLC
Country not established FDA FEI 3016661562
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Cro, LLC makes
Cro, LLC manufactures the AIRO Suction Unit (AIRO-01), a medical device designed for manual and automated suctioning of respiratory secretions in clinical settings.
The AIRO Suction Unit is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
AIRO Suction Unit (AIRO-01) Ref K251101
510(k) 510(k)
Company details
- FDA FEI number
- 3016661562
- Address
- 516 E. Spruce St., Missoula, MT, 59802
Frequently asked questions
How many devices does Cro, LLC have in the registry?
The registry currently lists 1 device for Cro, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cro, LLC's devices?
Among its 1 most recently registered device, Cro, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Cro, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Cro, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cro, LLC in the registry?
The most recently registered devices listed for Cro, LLC include AIRO Suction Unit (AIRO-01).