RecallHawk

Mobility Scooter (C4+)

Yongkang Yile Vehicle Co., Ltd.

Summary

Yongkang Yile Vehicle Co., Ltd. received 510(k) clearance for Mobility Scooter (C4+), a INI device. Cleared on 2024-04-18.

Details

Source

510(k) Clearance

External ID

K234098

Action Date

2024-04-18

Status

Traditional

Category

device

Product Code

INI

Product Description

Mobility Scooter (C4+). Product code: INI.

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. Yongkang Yile Vehicle Co., Ltd. has received 2 total clearances in our database.

Yongkang Yile Vehicle 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 Yongkang Yile Vehicle Co., Ltd. have FDA actions?

Yongkang Yile Vehicle 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 "K234098" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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