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FDA 510(k)

VARISOURCE 200 HDR AFTERLOADER

K-Number: K061582 · 2006-07-25

ApplicantVarian Medical Systems, Inc.
Decision Date2006-07-25
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VARISOURCE 200 HDR AFTERLOADER is the device name listed in this FDA 510(k) record. The listed applicant is Varian Medical Systems, Inc.. It received FDA 510(k) clearance on 2006-07-25 under 510(k) number K061582. 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 VARISOURCE 200 HDR AFTERLOADER?

VARISOURCE 200 HDR AFTERLOADER is a medical device that received FDA 510(k) clearance on 2006-07-25. The listed applicant is Varian Medical Systems, Inc.. The 510(k) number is K061582.

When did VARISOURCE 200 HDR AFTERLOADER receive FDA 510(k) clearance?

VARISOURCE 200 HDR AFTERLOADER received FDA 510(k) clearance on 2006-07-25, under 510(k) number K061582.

Who is the listed applicant for VARISOURCE 200 HDR AFTERLOADER?

The FDA 510(k) record lists Varian Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VARISOURCE 200 HDR AFTERLOADER?

The FDA product code for VARISOURCE 200 HDR AFTERLOADER is JAQ.

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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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