510(k) K212295
K212295 is an FDA 510(k) premarket notification submitted by Lg Electronics.Inc for the device "21HQ513D". The FDA issued a decision of Substantially Equivalent on Dec 3, 2021. The device falls under product code PGY (Display, Diagnostic Radiology), a Class II device regulated under 21 CFR 892.2050. Lg Electronics.Inc has 32 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Dec 3, 2021
- Date Received
- Jul 22, 2021
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Display, Diagnostic Radiology
- Device Class
- Class II
- Regulation Number
- 892.2050
- Review Panel
- RA
- Submission Type
- 510(k)
The device is intended for use in displaying radiological images for review, analysis, and diagnosis by trained medical practitioners.