RecallHawk

Parsortix PC1 Device

Angle Europe , Ltd.

Summary

Angle Europe , Ltd. received 510(k) clearance for Parsortix PC1 Device, a QSA device. Cleared on 2022-05-24.

Details

Source

510(k) Clearance

External ID

DEN200062

Action Date

2022-05-24

Status

Direct

Category

device

Product Code

QSA

Product Description

Parsortix PC1 Device. Product code: QSA.

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.

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 Angle Europe , Ltd. have FDA actions?

This is the only FDA action we have on record for Angle Europe , Ltd. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "DEN200062" 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