AOS UNIVERSAL CONNECTING GUIDE TUBE FOR HIGH DOSE RATE AFTERLOADERS— 510(k) K964910

Name: FDA 510(k) clearance K964910
Creator: U.S. Food and Drug Administration
Published: 1997-03-10

Substantially Equivalent

Alpha-Omega Services, Inc.

FDA 510(k) clearance K964910 for AOS UNIVERSAL CONNECTING GUIDE TUBE FOR HIGH DOSE RATE AFTERLOADERS, Substantially Equivalent on 1997-03-10. Applicant: Alpha-Omega Services, Inc.. Device class: 2.

Clearance details

Applicant: Alpha-Omega Services, Inc.
Product code: Code JAQ
Device class: Class 2
Regulation: 21 CFR 892.5700
Advisory panel: Radiology
Date received: 1996-12-09
Decision date: 1997-03-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bellflower, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JAQ

view all

K262383 — LumenCare Azure2026-07-24
K252717 — MAASTRO Rectal Applicator Set2026-05-20
K251037 — Rectal Applicator2025-12-19
K252884 — Guided Aarhus Applicator Set2025-11-19
K250299 — CT/ MR Tandem and Ovoid Set2025-05-09

More clearances from Alpha-Omega Services, Inc.

view all

K233628 — AOS Interstitial Templates, Needles, and Accessories2024-07-10
K233626 — AOS Marker Seeds (SMG0242-025)2024-07-02
K102811 — AOS ORION IR-192 SOURCE CABLE2011-06-02
K062824 — AOS UNIVERSAL CONECTING GUIDE TUBE2007-07-03
K062823 — AOS INTERSTITIAL TEMPLATES, NEEDLES & ACCESSORIES2007-05-29

Data sourced from openFDA. This site is unofficial and independent of the FDA.