CW120N

Display, Diagnostic Radiology

Wide Corporation

The following data is part of a premarket notification filed by Wide Corporation with the FDA for Cw120n.

Pre-market Notification Details

Device IDK210491
510k NumberK210491
Device Name:CW120N
ClassificationDisplay, Diagnostic Radiology
Applicant Wide Corporation 15F, The First Tower III, 602, Dongtangiheung-Ro Hwaseong-si,  KR 18469
ContactYeojin Yun
CorrespondentYeojin Yun
Wide Corporation 15F, The First Tower III, 602, Dongtangiheung-Ro Hwaseong-si,  KR 18469
Product CodePGY  
CFR Regulation Number892.2050 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2021-02-19
Decision Date2021-04-08

© 2021 FDA.report
This site is not affiliated with or endorsed by the FDA.