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Aardvark Medical

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K221664CLEARinse CTS Specimen Collection and Transport SystemJuly 3, 2023
K082762AARDVARK NASAL IRRIGATION AND ASPIRATION DEVICENovember 12, 2008