RecallHawk

colonic FTRD Set (200.70); diagnostic FTRD Set (200.76); gastroduodenal FTRD Set (200.72)

Ovesco Endoscopy AG

Summary

Ovesco Endoscopy AG received 510(k) clearance for colonic FTRD Set (200.70); diagnostic FTRD Set (200.76); gastroduodenal FTRD Set (200.72), a PKL device. Cleared on 2026-09-14.

Details

Source

510(k) Clearance

External ID

K253481

Action Date

2026-09-14

Status

Traditional

Category

device

Product Code

PKL

Product Description

colonic FTRD Set (200.70); diagnostic FTRD Set (200.76); gastroduodenal FTRD Set (200.72). Product code: PKL.

Context & Analysis

A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 445 device clearances issued this month. Ovesco Endoscopy AG has received 5 total clearances in our database.

Ovesco Endoscopy AG 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 Ovesco Endoscopy AG have FDA actions?

Ovesco Endoscopy AG 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 "K253481" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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