Cleared Special

Millipede70 Aspiration Catheter; Perfuze Aspiration Tube Set

K252392 · Perfuze, Ltd. · Neurology

Aug 2025

Decision

29d

Days

Class 2

Risk

About This 510(k) Submission

K252392 is an FDA 510(k) clearance for the Millipede70 Aspiration Catheter; Perfuze Aspiration Tube Set, a Catheter, Thrombus Retriever (Class II — Special Controls, product code NRY), submitted by Perfuze, Ltd. (Galway, IE). The FDA issued a Cleared decision on August 29, 2025, 29 days after receiving the submission on July 31, 2025. This device falls under the Neurology review panel. Regulated under 21 CFR 870.1250.

Submission Details

510(k) Number	K252392 FDA.gov
FDA Decision	Cleared SESE
Date Received	July 31, 2025
Decision Date	August 29, 2025
Days to Decision	29 days
Submission Type	Special
Review Panel	Neurology (NE)
Summary	Summary PDF

Device Classification

Product Code	NRY — Catheter, Thrombus Retriever
Device Class	Class II — Special Controls
CFR Regulation	21 CFR 870.1250
Definition	The Device Is Intended To Restore Blood Flow By Removing Thrombus/clots In Patients Experiencing Ischemic Stroke. The Prior Clearances In This Category Have Been Limited To Simply Identifying Catheter Placed In The Peripheral, Coronary, And Neurovasculature. It Is Felt That This Is A Unique Claim And Should Not Be Combined With Previously Cleared Catheters Under A General Procode.