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EVIS X1 VIDEO SYSTEM CENTER OLYMPUS CV-1500, COLONOVIDEOSCOPE OLYMPUS CF-HQ1100DL/I, GASTROINTESTINAL VIDEOSCOPE OLYMPUS

Olympus Medical Systems Corporation

Summary

Olympus Medical Systems Corporation received 510(k) clearance for EVIS X1 VIDEO SYSTEM CENTER OLYMPUS CV-1500, COLONOVIDEOSCOPE OLYMPUS CF-HQ1100DL/I, GASTROINTESTINAL VIDEOSCOPE OLYMPUS GIF-1100, a FET device. Cleared on 2023-04-26.

Details

Source

510(k) Clearance

External ID

K222584

Action Date

2023-04-26

Status

Traditional

Category

device

Product Code

FET

Product Description

EVIS X1 VIDEO SYSTEM CENTER OLYMPUS CV-1500, COLONOVIDEOSCOPE OLYMPUS CF-HQ1100DL/I, GASTROINTESTINAL VIDEOSCOPE OLYMPUS GIF-1100. Product code: FET.

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. Olympus Medical Systems Corporation has received 31 total clearances in our database.

Olympus Medical Systems Corporation has 31 FDA actions in our database, including 31 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 Olympus Medical Systems Corporation have FDA actions?

Olympus Medical Systems Corporation has 31 FDA actions in our database, including 0 recalls and 31 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K222584" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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