Everlife Medical Equipment Co., Ltd. is one of 632 FDA 510(k) medical device manufacturers from Taiwan in the dataset, ranked by real submission volume.
Everlife Medical Equipment Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: EVERELIFE TRANSCUTANEOUS MUSCLE STIMULATOR, EVERLIFE POWERED MUSCLE STIMULATOR, MODEL E-100204, E-100504, E-100509, E-100804, E-201111, E-201211, E-201311, EVERLIFE INTERFERENTIAL CURRENT THERAPY, MODEL IF-100507
3
Total
3
Cleared
0
Denied
Everlife Medical Equipment Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Hsin-Chu City, TW.
Historical record: 3 cleared submissions from 2007 to 2007. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Everlife Medical Equipment Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Everlife Medical Equipment Co., Ltd.
3 devices