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AZmed
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K243831
Rayvolve LN
March 26, 2025
K243808
Rayvolve PTX-PE
March 21, 2025
K240845
Rayvolve
July 17, 2024
K220164
Rayvolve
June 2, 2022