RecallHawk

Hybrid Viewer (00859873006240)

Hermes Medical Solutions AB

Summary

Hermes Medical Solutions AB received 510(k) clearance for Hybrid Viewer (00859873006240), a KPS device. Cleared on 2025-09-09.

Details

Source

510(k) Clearance

External ID

K252477

Action Date

2025-09-09

Status

Special

Category

device

Product Code

KPS

Product Description

Hybrid Viewer (00859873006240). Product code: KPS.

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. Hermes Medical Solutions AB has received 2 total clearances in our database.

Hermes Medical Solutions AB has 3 FDA actions in our database, including 1 recall and 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 Hermes Medical Solutions AB have FDA actions?

Hermes Medical Solutions AB has 3 FDA actions in our database, including 1 recall and 2 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K252477" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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