K233336
- 510(k) number
- K233336
- Device name
- 21.3 3MP Color LCD Display UMD3-21B01 (MD3-21B01)
- Applicant
- Acula Technology Corp. TW
- Product code
- PGY — Display, Diagnostic Radiology
- Decision date
- 2024-05-21
- Date received
- 2023-09-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 1.7 MB · U.S. public domain
Also available from FDA: K233336.pdf
Official FDA record: K233336
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.