Perfuze, Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
8
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K252392Millipede70 Aspiration Catheter; Perfuze Aspiration Tube SetAugust 29, 2025
K250012Millipede 070 Aspiration Catheter; Perfuze Aspiration Tube SetFebruary 26, 2025
K240711Zipline Access CatheterOctober 17, 2024
K242504Millipede 088 Access Catheter; Millipede 070 Aspiration Catheter; Perfuze Aspiration Tube SetSeptember 20, 2024
K233648Millipede 088 Access CatheterDecember 14, 2023
K232524Millipede 070 Aspiration Catheter; Perfuze Aspiration Tube SetOctober 18, 2023
K231802Millipede 088 Access CatheterSeptember 19, 2023
K214048Millipede 088 Access CatheterSeptember 20, 2022