K240130
- 510(k) number
- K240130
- Device name
- Medical Monitor (21HQ613D)
- Applicant
- Lg Electronics.Inc KR
- Product code
- PGY — Display, Diagnostic Radiology
- Decision date
- 2024-02-15
- Date received
- 2024-01-17
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Radiology
510(k) Summary (official FDA PDF): K240130.pdf
Official FDA record: K240130
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.