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FDA 510(k)

VARISOURCE BREAST TEMPLATE SYSTEM

K-Number: K023220 · 2002-10-25

ApplicantVarian Medical Systems
Decision Date2002-10-25
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VARISOURCE BREAST TEMPLATE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Varian Medical Systems. It received FDA 510(k) clearance on 2002-10-25 under 510(k) number K023220. 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 BREAST TEMPLATE SYSTEM?

VARISOURCE BREAST TEMPLATE SYSTEM is a medical device that received FDA 510(k) clearance on 2002-10-25. The listed applicant is Varian Medical Systems. The 510(k) number is K023220.

When did VARISOURCE BREAST TEMPLATE SYSTEM receive FDA 510(k) clearance?

VARISOURCE BREAST TEMPLATE SYSTEM received FDA 510(k) clearance on 2002-10-25, under 510(k) number K023220.

Who is the listed applicant for VARISOURCE BREAST TEMPLATE SYSTEM?

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

What is the FDA product code for VARISOURCE BREAST TEMPLATE SYSTEM?

The FDA product code for VARISOURCE BREAST TEMPLATE SYSTEM is JAQ.

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Other records listing Varian Medical Systems 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.

K261306AI Contouring (VA10A)K252717MAASTRO Rectal Applicator SetK252884Guided Aarhus Applicator SetK250099Mobius3D (4.1)K250289Intracavitary/Interstitial SystemK242378Eclipse Treatment Planning System (18.1)

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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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