TRILOGY MX

Accelerator, Linear, Medical

VARIAN MEDICAL SYSTEMS, INC.

The following data is part of a premarket notification filed by Varian Medical Systems, Inc. with the FDA for Trilogy Mx.

Pre-market Notification Details

Device IDK092871
510k NumberK092871
Device Name:TRILOGY MX
ClassificationAccelerator, Linear, Medical
Applicant VARIAN MEDICAL SYSTEMS, INC. 3100 HANSEN WAY Palo Alto,  CA  94304
ContactVy Tran
CorrespondentVy Tran
VARIAN MEDICAL SYSTEMS, INC. 3100 HANSEN WAY Palo Alto,  CA  94304
Product CodeIYE  
CFR Regulation Number892.5050 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2009-09-18
Decision Date2009-11-30
Summary:summary

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