K231764
- 510(k) number
- K231764
- Device name
- Ultrasound System 1300
- Applicant
- Bk Medical Aps DK
- Product code
- IYN — System, Imaging, Pulsed Doppler, Ultrasonic
- Decision date
- 2023-10-23
- Date received
- 2023-06-16
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K231764.pdf
Official FDA record: K231764
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.