K232302
- 510(k) number
- K232302
- Device name
- Pocket III
- Applicant
- Quantel Medical FR
- Product code
- IYO — System, Imaging, Pulsed Echo, Ultrasonic
- Decision date
- 2024-04-26
- Date received
- 2023-08-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K232302.pdf
Official FDA record: K232302
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.