meddevicedb.com FDA Device Reference

AOS Marker Seeds (SMG0242-025)

K233626 Class II Traditional
Decision Date
2024-07-02
Sponsor / Applicant
Alpha-Omega Services, Inc.

Technical Specification

510(k) Submission ID K233626
Product Code JAQ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5700
Decision Date 2024-07-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AOS Marker Seeds (SMG0242-025) received FDA 510(k) clearance under submission number K233626, sponsored by Alpha-Omega Services, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2024-07-02.

Classification & Regulation

This clearance is catalogued under FDA product code JAQ and 21 CFR 892.5700, within the Radiology review panel as a Class II device.