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FDA 510(k)

AOS UNIVERSAL CONECTING GUIDE TUBE

K-Number: K062824 · 2007-07-03

ApplicantAlpha-Omega Services, Inc.
Decision Date2007-07-03
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AOS UNIVERSAL CONECTING GUIDE TUBE 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 2007-07-03 under 510(k) number K062824. 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 UNIVERSAL CONECTING GUIDE TUBE?

AOS UNIVERSAL CONECTING GUIDE TUBE is a medical device that received FDA 510(k) clearance on 2007-07-03. The listed applicant is Alpha-Omega Services, Inc.. The 510(k) number is K062824.

When did AOS UNIVERSAL CONECTING GUIDE TUBE receive FDA 510(k) clearance?

AOS UNIVERSAL CONECTING GUIDE TUBE received FDA 510(k) clearance on 2007-07-03, under 510(k) number K062824.

Who is the listed applicant for AOS UNIVERSAL CONECTING GUIDE TUBE?

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 UNIVERSAL CONECTING GUIDE TUBE?

The FDA product code for AOS UNIVERSAL CONECTING GUIDE TUBE is JAQ.

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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 AccessoriesK233626AOS Marker Seeds (SMG0242-025)K102811AOS ORION IR-192 SOURCE CABLEK062823AOS INTERSTITIAL TEMPLATES, NEEDLES & ACCESSORIESK062825AOS MARKER SEEDSK062826AOS IMPLANT TUBES, IMPLANT NEEDLES & RETAINING BOTTONS

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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.

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