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/ Palliare , Ltd.
Palliare , Ltd.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
6
Inspections
1
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K232902
EVA15 insufflator
May 2, 2024
K230474
EVA5 Insufflator
March 24, 2023
K222901
EVA15 insufflator
January 27, 2023
K202922
END 200 Endoscopic Tubeset
July 8, 2021
K202799
EVA15
October 21, 2020
K193520
EVA 15 Insufflator
July 23, 2020