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FDA 510(k)

TRILOGY SYSTEM WITH RAPIDARC

K-Number: K072916 · 2007-11-09

ApplicantVarian Medical Systems, Inc.
Decision Date2007-11-09
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TRILOGY SYSTEM WITH RAPIDARC 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 2007-11-09 under 510(k) number K072916. 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 SYSTEM WITH RAPIDARC?

TRILOGY SYSTEM WITH RAPIDARC is a medical device that received FDA 510(k) clearance on 2007-11-09. The listed applicant is Varian Medical Systems, Inc.. The 510(k) number is K072916.

When did TRILOGY SYSTEM WITH RAPIDARC receive FDA 510(k) clearance?

TRILOGY SYSTEM WITH RAPIDARC received FDA 510(k) clearance on 2007-11-09, under 510(k) number K072916.

Who is the listed applicant for TRILOGY SYSTEM WITH RAPIDARC?

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 SYSTEM WITH RAPIDARC?

The FDA product code for TRILOGY SYSTEM WITH RAPIDARC 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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