Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

AOS Marker Seeds (SMG0242-025)

K-Number: K233626 · 2024-07-02

ApplicantAlpha-Omega Services, Inc.
Decision Date2024-07-02
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AOS Marker Seeds (SMG0242-025) is the device name listed in this FDA 510(k) record. The listed applicant is Alpha-Omega Services, Inc.. It received FDA 510(k) clearance on 2024-07-02 under 510(k) number K233626. The device is classified under product code JAQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AOS Marker Seeds (SMG0242-025)?

AOS Marker Seeds (SMG0242-025) is a medical device that received FDA 510(k) clearance on 2024-07-02. The listed applicant is Alpha-Omega Services, Inc.. The 510(k) number is K233626.

When did AOS Marker Seeds (SMG0242-025) receive FDA 510(k) clearance?

AOS Marker Seeds (SMG0242-025) received FDA 510(k) clearance on 2024-07-02, under 510(k) number K233626.

Who is the listed applicant for AOS Marker Seeds (SMG0242-025)?

The FDA 510(k) record lists Alpha-Omega Services, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AOS Marker Seeds (SMG0242-025)?

The FDA product code for AOS Marker Seeds (SMG0242-025) is JAQ.

Other records listing Alpha-Omega Services, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K233628AOS Interstitial Templates, Needles, and Accessories

Related Devices (Code: JAQ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K262383LumenCare AzureNucletron B.V.K252717MAASTRO Rectal Applicator SetVarian Medical SystemsK251037Rectal ApplicatorNucletron B.V.K252884Guided Aarhus Applicator SetVarian Medical SystemsK250299CT/ MR Tandem and Ovoid SetVarian Medical Systems, Inc.K250289Intracavitary/Interstitial SystemVarian Medical Systems

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑