6MV PORT FILM CAPABILITY OPTION

Accelerator, Linear, Medical

VARIAN ASSOC., INC.

The following data is part of a premarket notification filed by Varian Assoc., Inc. with the FDA for 6mv Port Film Capability Option.

Pre-market Notification Details

Device IDK802808
510k NumberK802808
Device Name:6MV PORT FILM CAPABILITY OPTION
ClassificationAccelerator, Linear, Medical
Applicant VARIAN ASSOC., INC. 4221 Richmond Rd., N.W. Walker,  MI  49534
Product CodeIYE  
CFR Regulation Number892.5050 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1980-11-07
Decision Date1981-01-07

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