510(k) K232536

Device
Soldier Microcatheter
Applicant
Embolx, Inc.
510(k) number
K232536
Product code
DQO
Decision
Substantially Equivalent (SESE)
Decision date
2024-02-23
Date received
2023-08-21
Regulation
870.1200
Classification name
Catheter, Intravascular, Diagnostic
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Louise Musante
Address
530 Lakeside Dr. Suite 200 Sunnyvale CA US 94085 94085

FDA Registration Numbers

Source Documents

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

Other 510(k) Records For Product Code DQO

510(k)DeviceApplicantDecision date
K254278Arterial Pressure Monitoring Set/TraySpectrum Vascular2026-03-25
K250751DualView CatheterTerumo Corporation2025-07-17
K242966Gentuity® HF-OCT Imaging System with Vis-Rx Prime® Micro-Imaging CatheterGentuity, LLC2025-01-31
K242420pNOVUS 21 MicrocatheterPhenox, Ltd.2024-11-12
K233268Impress Angiographic CatheterMerit Medical Systems, Inc.2024-05-22
K233975Zoom 6F Insert CathetersImperative Care, Inc.2024-04-02
K232573INFINITI™ Ambi Angiographic CatheterCordis US Corp2023-11-21
K230620Gentuity® HF-OCT Imaging System with Vis-Rx® Micro-Imaging CatheterGentuity, LLC2023-08-08
K231293Drakon™ and Sequre® MicrocathetersAccurate Medical Therapeutics2023-06-01
K230411Dragonfly OpStar™ Imaging CatheterABBOTT MEDICAL2023-04-14
K221279pNOVUS 21 MicrocatheterPhenox, Ltd.2022-11-28
K213666NuCath Wedge Pressure CatheterPfm Medical, Inc.2022-10-06
K221470Langston dual lumen catheterVascular Solutions, LLC2022-06-17
K212977SUPER TORQUE MB Angiographic Catheter with Radiopaque markerbandsCordis Corporation2022-02-17
K211078Progreat LambdaTerumo Clinical Supply Co., Ltd.2021-12-21