RecallHawk

AOS Marker Seeds (SMG0242-025)

Alpha-Omega Services, Inc.

Summary

Alpha-Omega Services, Inc. received 510(k) clearance for AOS Marker Seeds (SMG0242-025), a JAQ device. Cleared on 2024-07-02.

Details

Source

510(k) Clearance

External ID

K233626

Action Date

2024-07-02

Status

Traditional

Category

device

Product Code

JAQ

Product Description

AOS Marker Seeds (SMG0242-025). Product code: JAQ.

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. Alpha-Omega Services, Inc. has received 2 total clearances in our database.

Alpha-Omega Services, Inc. has 2 FDA actions in our database, including 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 Alpha-Omega Services, Inc. have FDA actions?

Alpha-Omega Services, Inc. has 2 FDA actions in our database, including 0 recalls and 2 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K233626" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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