510(k) K252392

Device
Millipede70 Aspiration Catheter; Perfuze Aspiration Tube Set
Applicant
Perfuze, Ltd.
510(k) number
K252392
Product code
NRY
Decision
Substantially Equivalent (SESE)
Decision date
2025-08-29
Date received
2025-07-31
Regulation
870.1250
Classification name
Catheter, Thrombus Retriever
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Anne-Marie Gannon
Address
Unit 6, Galway Business Park Dangan Galway IE H91W7CP H91W7CP

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

Other 510(k) Records For Product Code NRY

510(k)DeviceApplicantDecision date
K254276Lynx Aspiration Catheter SystemQ’Apel Medical, Inc.2026-05-07
K253590Millipede SystemPerfuze, Ltd.2026-03-16
K253062Tigertriever 25 Revascularization DeviceRapid Medical , Ltd.2026-03-12
K251357Esperance pHLO Aspiration SystemPhenox, Ltd.2026-01-15
K251006NeVasc Aspiration SystemVesalio, Inc.2025-11-10
K252046Zoom System (Zoom 4S Catheter)Imperative Care, Inc.2025-10-30
K251603Tigertriever 17 Ultra Revascularization DeviceRapid Medical , Ltd.2025-10-06
K251789EMBOTRAP III Revascularization DeviceNeuravi Limited2025-09-25
K251828CEREGLIDE 71 Catheter System; Cerenovus Aspiration Tubing SetCerenovus, Inc.2025-08-22
K243948Raptor Aspiration Catheter; Balt Aspiration Tubing SetBalt USA, LLC2025-06-03
K243047Zoom 7X Catheter; Zoom Aspiration Tubing; Zoom POD Aspiration TubingImperative Care, Inc.2025-05-28
K243601Route 92 Medical HiPoint Reperfusion System and Aspiration Tubing SetRoute 92 Medical, Inc.2025-05-19
K251015APRO 45 Catheter and Alembic Aspiration TubingAlembic, LLC2025-04-30
K250958APRO 55 Swift Catheter and Alembic Aspiration TubingAlembic, LLC2025-04-28
K250012Millipede 070 Aspiration Catheter; Perfuze Aspiration Tube SetPerfuze, Ltd.2025-02-26