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SUPER TORQUE MB Angiographic Catheter with Radiopaque markerbands

Cordis Corporation

Summary

Cordis Corporation received 510(k) clearance for SUPER TORQUE MB Angiographic Catheter with Radiopaque markerbands, a DQO device. Cleared on 2022-02-17.

Details

Source

510(k) Clearance

External ID

K212977

Action Date

2022-02-17

Status

Traditional

Category

device

Product Code

DQO

Product Description

SUPER TORQUE MB Angiographic Catheter with Radiopaque markerbands. Product code: DQO.

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. Cordis Corporation has received 2 total clearances in our database.

Cordis Corporation has 15 FDA actions in our database, including 13 recalls and 2 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 Cordis Corporation have FDA actions?

Cordis Corporation has 15 FDA actions in our database, including 13 recalls and 2 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K212977" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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