RecallHawk

C630G LCD monitor, JUSHA-C630G LCD monitor, C630 LCD monitor, JUSHA-C630 LCD monitor

Nanjing Jusha Display Technology Co., Ltd.

Summary

Nanjing Jusha Display Technology Co., Ltd. received 510(k) clearance for C630G LCD monitor, JUSHA-C630G LCD monitor, C630 LCD monitor, JUSHA-C630 LCD monitor, a PGY device. Cleared on 2022-09-19.

Details

Source

510(k) Clearance

External ID

K222121

Action Date

2022-09-19

Status

Traditional

Category

device

Product Code

PGY

Product Description

C630G LCD monitor, JUSHA-C630G LCD monitor, C630 LCD monitor, JUSHA-C630 LCD monitor. Product code: PGY.

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. Nanjing Jusha Display Technology Co., Ltd. has received 5 total clearances in our database.

Nanjing Jusha Display Technology Co., Ltd. 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 Nanjing Jusha Display Technology Co., Ltd. have FDA actions?

Nanjing Jusha Display Technology Co., Ltd. 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 "K222121" 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