SOMATOM SD

System, X-ray, Tomography, Computed

SIEMENS CORP.

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

Pre-market Notification Details

Device IDK790342
510k NumberK790342
Device Name:SOMATOM SD
ClassificationSystem, X-ray, Tomography, Computed
Applicant SIEMENS CORP. 4221 Richmond Rd., N.W. Walker,  MI  49534
Product CodeJAK  
CFR Regulation Number892.1750 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1979-02-21
Decision Date1979-03-22

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