CLINAC 2500

Accelerator, Linear, Medical

VARIAN ASSOC., INC.

The following data is part of a premarket notification filed by Varian Assoc., Inc. with the FDA for Clinac 2500.

Pre-market Notification Details

Device IDK781872
510k NumberK781872
Device Name:CLINAC 2500
ClassificationAccelerator, Linear, Medical
Applicant VARIAN ASSOC., INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeIYE  
CFR Regulation Number892.5050 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1978-11-03
Decision Date1978-11-27

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