NaviCam ProScan— 510(k) DEN230027

Unknown

Ankon Technologies Co., Ltd.

FDA 510(k) clearance DEN230027 for NaviCam ProScan, Unknown on 2023-12-12. Applicant: Ankon Technologies Co., Ltd.. Device class: 2.

Clearance details

Applicant: Ankon Technologies Co., Ltd.
Product code: Code QZF
Device class: Class 2
Regulation: 21 CFR 876.1540
Advisory panel: Gastroenterology, Urology
Date received: 2023-04-14
Decision date: 2023-12-12
Decision: Unknown
Clearance type: Direct
Location: Wuhan, CN

View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.