Apollon Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Apollon Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Foley Balloon Catheter for Urology
1
Total
1
Cleared
0
Denied
Apollon Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Incheon, KR.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Apollon Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tsd Life Sciences Co., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Apollon Co., Ltd.
1 devices