XIMATRON V

System, Simulation, Radiation Therapy

SIEMENS CORP.

The following data is part of a premarket notification filed by Siemens Corp. with the FDA for Ximatron V.

Pre-market Notification Details

Device IDK810858
510k NumberK810858
Device Name:XIMATRON V
ClassificationSystem, Simulation, Radiation Therapy
Applicant SIEMENS CORP. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeKPQ  
CFR Regulation Number892.5840 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1981-03-30
Decision Date1981-05-13

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.