K261213
- 510(k) number
- K261213
- Device name
- Medical Monitor (40HT513D)
- Applicant
- Lg Electronics.Inc KR
- Product code
- PGY — Display, Diagnostic Radiology
- Decision date
- 2026-06-12
- Date received
- 2026-04-14
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K261213.pdf
Official FDA record: K261213
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.