Astel, Inc. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Astel, Inc. - FDA 510(k) Cleared Devices
Recent clearances: RFA-1717DIG, RFA-1717DIC
1
Total
1
Cleared
0
Denied
Astel, Inc. has 1 FDA 510(k) cleared medical devices. Based in Daejeon, KR.
Last cleared in 2021. Active since 2021. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Astel, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mtechgroup as regulatory consultant.
FDA 510(k) Regulatory Record - Astel, Inc.
1 devices