FDA 510(k)

Toro 88 Superbore Catheter

K-Number: K252297 · 2026-01-16

Decision Date2026-01-16

Product CodeQJP

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

Toro 88 Superbore Catheter is a medical device manufactured by Toro Neurovascular, Inc.. It received FDA 510(k) clearance on 2026-01-16 under approval number K252297. The device is classified under product code QJP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Toro 88 Superbore Catheter?

Toro 88 Superbore Catheter is a medical device that received FDA 510(k) clearance on 2026-01-16. It is manufactured by Toro Neurovascular, Inc.. The 510(k) number is K252297.

When was Toro 88 Superbore Catheter approved by the FDA?

Toro 88 Superbore Catheter received FDA 510(k) clearance on 2026-01-16, under approval number K252297.

What company makes Toro 88 Superbore Catheter?

Toro 88 Superbore Catheter is manufactured by Toro Neurovascular, Inc..

What is the FDA product code for Toro 88 Superbore Catheter?

The FDA product code for Toro 88 Superbore Catheter is QJP.

Related Devices (Code: QJP)

K203043Route 92 Medical 070 Access SystemRoute 92 Medical, Inc. K201682RIST Radial Access CatheterRist Neurovascular, Inc. K201518Route 92 Medical 088 Access SystemRoute 92 Medical K201076Anchor Dual Lumen Guidewire CatheterAqure Medical, Inc. K200910BOSS Balloon Guide CatheterMarblehead Medical K200417RIST Radial Access CatheterRist Neurovascular, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.