ClearanceBrief
Company ยท IL

Dia Imaging Analysis, Ltd.

FDA 510(k) clearances and medical device recalls filed under this name, 2020 to 2025. Name variants (Inc, Corp, punctuation) are merged.

10510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
QIHAutomated Radiological Image Processing Software10

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Mar 17, 2025K243862LVivo Software Application
Dia Imaging Analysis, Ltd., IL
QIH
Mar 6, 2025K243331LVivo Seamless
Dia Imaging Analysis, Ltd., IL
QIH
Mar 3, 2025K243235LVivo Software Application
Dia Imaging Analysis, Ltd., IL
QIH
Oct 4, 2024K240553LVivo Software Application
Dia Imaging Analysis, Ltd., IL
QIH
May 24, 2024K240769LVivo IQS
Dia Imaging Analysis, Ltd., IL
QIH
Feb 1, 2023K222970LVivo IQS
Dia Imaging Analysis, Ltd., IL
QIH
Dec 9, 2021K212466LVivo Seamless
Dia Imaging Analysis, Ltd., IL
QIH
Feb 5, 2021K210053LVivo Software Application
Dia Imaging Analysis, Ltd., IL
QIH
Sep 29, 2020K202546LVivo Seamless
Dia Imaging Analysis, Ltd., IL
QIH
Jun 23, 2020K200232LVivo Software Application
Dia Imaging Analysis, Ltd., IL
QIH

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes