Angeline Group , Ltd. is one of 203 FDA 510(k) medical device manufacturers from Taiwan in the dataset, ranked by real submission volume.
Angeline Group , Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Angeline Group , Ltd. has 1 FDA 510(k) cleared medical devices. Based in New Taipei City, TW.
Historical record: 1 cleared submissions from 2011 to 2011. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Angeline Group , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Angeline Group , Ltd.
1 devices