Medical Device Manufacturer · IE , Galway

Perfuze, Ltd. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 2022
9
Total
9
Cleared
0
Denied
FDA 510(k) Regulatory Record - Perfuze, Ltd. Neurology ✕
9 devices
1-9 of 9
Cleared CT Mar 16, 2026
Millipede System
K253590 · NRY
Neurology · 119d
Cleared Aug 29, 2025
Millipede70 Aspiration Catheter
K252392 · NRY
Neurology · 29d
Cleared Feb 26, 2025
Millipede 070 Aspiration Catheter
K250012 · NRY
Neurology · 55d
Cleared Oct 17, 2024
Zipline Access Catheter
K240711 · QJP
Neurology · 216d
Cleared Sep 20, 2024
Millipede 088 Access Catheter
K242504 · NRY
Neurology · 29d
Cleared Dec 14, 2023
Millipede 088 Access Catheter
K233648 · QJP
Neurology · 30d
Cleared Oct 18, 2023
Millipede 070 Aspiration Catheter
K232524 · NRY
Neurology · 61d
Cleared Sep 19, 2023
Millipede 088 Access Catheter
K231802 · QJP
Neurology · 91d
Cleared Sep 20, 2022
Millipede 088 Access Catheter
K214048 · QJP
Neurology · 267d
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