Ankon Technologies Co., Ltd. - FDA 510(k) Cleared Devices
2
Total
1
Cleared
1
Denied
Ankon Technologies Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Wuhan, CN.
Last cleared in 2022. Active since 2022. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Ankon Technologies Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by ProMedoss, Inc. as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
2 devices