RecallHawk

FilmArray GI Control Panel M238

Maine Molecular Quality Controls, Inc.

Summary

Maine Molecular Quality Controls, Inc. received 510(k) clearance for FilmArray GI Control Panel M238, a PMN device. Cleared on 2025-08-14.

Details

Source

510(k) Clearance

External ID

K251526

Action Date

2025-08-14

Status

Traditional

Category

device

Product Code

PMN

Product Description

FilmArray GI Control Panel M238. Product code: PMN.

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. Maine Molecular Quality Controls, Inc. has received 7 total clearances in our database.

Maine Molecular Quality Controls, Inc. has 7 FDA actions in our database, including 7 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 Maine Molecular Quality Controls, Inc. have FDA actions?

Maine Molecular Quality Controls, Inc. has 7 FDA actions in our database, including 0 recalls and 7 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K251526" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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