DEN230027
- 510(k) number
- DEN230027
- Device name
- NaviCam ProScan
- Applicant
- Ankon Technologies Co., Ltd. CN
- Product code
- QZF — Gastrointestinal Capsule Endoscopy Analysis Software
- Decision date
- 2023-12-12
- Date received
- 2023-04-14
- Decision
- Unknown
- Clearance type
- Direct
- Advisory committee
- Gastroenterology, Urology
Official FDA record: DEN230027
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.