Aardvark Medical
Country not established
- Devices
- 2
What Aardvark Medical makes
Aardvark Medical manufactures the Aardvark Nasal Irrigation and Aspiration Device, designed for clearing nasal passages and managing secretions in patients.
The device is classified as Class II under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
- 510(k) 510(k)
Aardvark Nasal Irrigation And Aspiration Device Ref K082762
510(k) 510(k)
Frequently asked questions
How many devices does Aardvark Medical have in the registry?
The registry currently lists 2 devices for Aardvark Medical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aardvark Medical's devices?
Among its 2 most recently registered devices, Aardvark Medical has devices listed in FDA 510(k) (2 devices).
What risk classes do Aardvark Medical's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Aardvark Medical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Aardvark Medical in the registry?
The most recently registered devices listed for Aardvark Medical include CLEARinse CTS Specimen Collection and Transport System and AARDVARK NASAL IRRIGATION AND ASPIRATION DEVICE.