Avitro, LLC
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Avitro, LLC makes
Avitro, LLC manufactures heparin sodium in 10 and 100 USO units/mL formulations and 0.9% sodium chloride vascular access devices.
These products are classified as Class II medical devices and are listed under FDA 510(k) clearance. The company is based in the United States.
Catalogue
- 510(k) 510(k)
0.9% Sodium Chloride Vasculat Access Device Ref K000632
510(k) 510(k)
Frequently asked questions
How many devices does Avitro, LLC have in the registry?
The registry currently lists 2 devices for Avitro, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Avitro, LLC's devices?
Among its 2 most recently registered devices, Avitro, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Avitro, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Avitro, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Avitro, LLC in the registry?
The most recently registered devices listed for Avitro, LLC include THE AVITRO LLC, 10 AND 100 USO UNITS/ML HEPARIN SODIUM VAFD and 0.9% SODIUM CHLORIDE VASCULAT ACCESS DEVICE.