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FDA 510(k)

AOS UNIVERSAL CONNECTING GUIDE TUBE FOR HIGH DOSE RATE AFTERLOADERS

K-Number: K964910 · 1997-03-10

ApplicantAlpha-Omega Services, Inc.
Decision Date1997-03-10
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AOS UNIVERSAL CONNECTING GUIDE TUBE FOR HIGH DOSE RATE AFTERLOADERS 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 1997-03-10 under 510(k) number K964910. 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 CONNECTING GUIDE TUBE FOR HIGH DOSE RATE AFTERLOADERS?

AOS UNIVERSAL CONNECTING GUIDE TUBE FOR HIGH DOSE RATE AFTERLOADERS is a medical device that received FDA 510(k) clearance on 1997-03-10. The listed applicant is Alpha-Omega Services, Inc.. The 510(k) number is K964910.

When did AOS UNIVERSAL CONNECTING GUIDE TUBE FOR HIGH DOSE RATE AFTERLOADERS receive FDA 510(k) clearance?

AOS UNIVERSAL CONNECTING GUIDE TUBE FOR HIGH DOSE RATE AFTERLOADERS received FDA 510(k) clearance on 1997-03-10, under 510(k) number K964910.

Who is the listed applicant for AOS UNIVERSAL CONNECTING GUIDE TUBE FOR HIGH DOSE RATE AFTERLOADERS?

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 CONNECTING GUIDE TUBE FOR HIGH DOSE RATE AFTERLOADERS?

The FDA product code for AOS UNIVERSAL CONNECTING GUIDE TUBE FOR HIGH DOSE RATE AFTERLOADERS 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 CABLEK062824AOS UNIVERSAL CONECTING GUIDE TUBEK062823AOS INTERSTITIAL TEMPLATES, NEEDLES & ACCESSORIESK062825AOS MARKER SEEDS

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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.

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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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