RecallHawk

SC1 Handheld Ultrasound Imaging System (Model: SC1)

Fcu Co., Ltd.

Summary

Fcu Co., Ltd. received 510(k) clearance for SC1 Handheld Ultrasound Imaging System (Model: SC1), a IYO device. Cleared on 2021-07-23.

Details

Source

510(k) Clearance

External ID

K210468

Action Date

2021-07-23

Status

Traditional

Category

device

Product Code

IYO

Product Description

SC1 Handheld Ultrasound Imaging System (Model: SC1). Product code: IYO.

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. Fcu Co., Ltd. has received 2 total clearances in our database.

Fcu Co., Ltd. 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 Fcu Co., Ltd. have FDA actions?

Fcu Co., Ltd. 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 "K210468" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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