K232336
- 510(k) number
- K232336
- Device name
- ES Series V2
- Applicant
- E-Scopics FR
- Product code
- IYN — System, Imaging, Pulsed Doppler, Ultrasonic
- Decision date
- 2023-09-26
- Date received
- 2023-08-04
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 1.2 MB · U.S. public domain
Also available from FDA: K232336.pdf
Official FDA record: K232336
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.