510(k) K223789

Device
21HQ513D
Applicant
Lg Electronics.Inc
510(k) number
K223789
Product code
PGY
Decision
Substantially Equivalent (SESE)
Decision date
2023-01-09
Date received
2022-12-19
Regulation
892.2050
Classification name
Display, Diagnostic Radiology
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Jinhwan Jun
Address
168, Suchul-Daero Gumi-Si KR 39368 39368

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

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