K231783
- 510(k) number
- K231783
- Device name
- VitroPRO
- Applicant
- CIVCO Medical Instruments Co., Inc. IA · US
- Product code
- ITX — Transducer, Ultrasonic, Diagnostic
- Decision date
- 2023-11-14
- Date received
- 2023-06-16
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Radiology
510(k) Summary (official FDA PDF): K231783.pdf
Official FDA record: K231783
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.