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FDA 510(k)

TRILOGY RADIOTHERAPY DELIVERY SYSTEM

K-Number: K033343 · 2003-12-23

ApplicantVarian Medical Systems, Inc.
Decision Date2003-12-23
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TRILOGY RADIOTHERAPY DELIVERY SYSTEM 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 2003-12-23 under 510(k) number K033343. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRILOGY RADIOTHERAPY DELIVERY SYSTEM?

TRILOGY RADIOTHERAPY DELIVERY SYSTEM is a medical device that received FDA 510(k) clearance on 2003-12-23. The listed applicant is Varian Medical Systems, Inc.. The 510(k) number is K033343.

When did TRILOGY RADIOTHERAPY DELIVERY SYSTEM receive FDA 510(k) clearance?

TRILOGY RADIOTHERAPY DELIVERY SYSTEM received FDA 510(k) clearance on 2003-12-23, under 510(k) number K033343.

Who is the listed applicant for TRILOGY RADIOTHERAPY DELIVERY SYSTEM?

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 TRILOGY RADIOTHERAPY DELIVERY SYSTEM?

The FDA product code for TRILOGY RADIOTHERAPY DELIVERY SYSTEM is IYE.

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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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