Well-Life Healthcare, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
FDA 510(k) Regulatory Record - Well-Life Healthcare, Inc. Neurology ✕
5 devices
Cleared
May 27, 2004
LIMITED FUNCTION WL/OTC-TENS DEVICE, MODEL WL-2103A, WL-2203A, WL-2203B AND...
Neurology
90d
Cleared
Dec 19, 2003
T-TECH DIGITAL, MODEL WL-22XXA SERIES
Neurology
8d
Cleared
Mar 20, 2003
DIGI-PRO TENS/WL-2203B,2204B,2204B-P1,2204B-P2,2205B
Neurology
28d
Cleared
Dec 30, 2002
THE IZZZY-TENS (WL-2401), THE SLIM-TENS (WL-2402), THE MENS-TENS (WL2403),...
Neurology
361d
Cleared
Apr 30, 2002
DIGI-PRO TENS MODEL WL-2203 AND WL-2205
Neurology
90d