RecallHawk

FETOLY-HEART

Diagnoly

Summary

Diagnoly received 510(k) clearance for FETOLY-HEART, a IYN device. Cleared on 2024-09-11.

Details

Source

510(k) Clearance

External ID

K241380

Action Date

2024-09-11

Status

Traditional

Category

device

Product Code

IYN

Product Description

FETOLY-HEART. Product code: IYN.

Company

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. Diagnoly has received 2 total clearances in our database.

Diagnoly has 2 FDA actions in our database, including 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 Diagnoly have FDA actions?

Diagnoly has 2 FDA actions in our database, including 0 recalls and 2 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K241380" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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