RecallHawk

Rist 079 Radial Access Guide Catheter; Rist 071 Radial Access Guide Catheter; Rist Radial Access Selective Catheter

Micro Therapeutics, Inc. d/b/a ev3 Neurovascular

Summary

Micro Therapeutics, Inc. d/b/a ev3 Neurovascular received 510(k) clearance for Rist 079 Radial Access Guide Catheter; Rist 071 Radial Access Guide Catheter; Rist Radial Access Selective Catheter, a QJP device. Cleared on 2025-01-02.

Details

Source

510(k) Clearance

External ID

K241388

Action Date

2025-01-02

Status

Special

Category

device

Product Code

QJP

Product Description

Rist 079 Radial Access Guide Catheter; Rist 071 Radial Access Guide Catheter; Rist Radial Access Selective Catheter. Product code: QJP.

Context & Analysis

A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 403 device clearances issued this month. Micro Therapeutics, Inc. d/b/a ev3 Neurovascular has received 5 total clearances in our database.

Micro Therapeutics, Inc. d/b/a ev3 Neurovascular has 5 FDA actions in our database, including 5 clearances.

Frequently Asked Questions

What does 510(k) clearance mean?

A 510(k) is an FDA premarket submission demonstrating that a device is substantially equivalent to a legally marketed device. It does NOT mean FDA approval — it means the device is cleared for marketing because it's similar enough to an existing cleared device. Most medical devices reach market via 510(k) rather than full PMA approval.

How often does Micro Therapeutics, Inc. d/b/a ev3 Neurovascular have FDA actions?

Micro Therapeutics, Inc. d/b/a ev3 Neurovascular has 5 FDA actions in our database, including 0 recalls and 5 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K241388" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for device

Related Actions