Aardvark Medical is one of 24903 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aardvark Medical - FDA 510(k) Cleared Devices
Recent clearances: AARDVARK NASAL IRRIGATION AND ASPIRATION DEVICE
1
Total
1
Cleared
0
Denied
Aardvark Medical has 1 FDA 510(k) cleared medical devices. Based in Ross, US.
Historical record: 1 cleared submissions from 2008 to 2008. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Aardvark Medical Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Aardvark Medical
1 devices