510(k) K241388

Device
Rist 079 Radial Access Guide Catheter; Rist 071 Radial Access Guide Catheter; Rist Radial Access Selective Catheter
Applicant
Micro Therapeutics, Inc. d/b/a ev3 Neurovascular
510(k) number
K241388
Product code
QJP
Decision
Substantially Equivalent (SESE)
Decision date
2025-01-02
Date received
2024-05-15
Regulation
870.1250
Classification name
Catheter, Percutaneous, Neurovasculature
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Vesselina Clayton
Address
9775 Toledo Way Irvine CA US 92618 92618

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code QJP#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
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K252297Toro 88 Superbore CatheterToro Neurovascular, Inc.2026-01-16
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K251668SurfRider 13 MicrocatheterKaneka Americas Holding, Inc.2026-01-05
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K251372VersaD Delivery CatheterUnity Medical, Inc.2025-10-24
K252569Carrier XL Delivery CatheterBalt USA, LLC2025-10-22
K250960DUO MicrocatheterRev Neuro, LLC2025-09-08
K251560FUBUKI XF-R Neurovascular Long SheathAsahi Intecc Co., Ltd.2025-06-20