Well-Life Healthcare, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DIGI-PRO TENS/WL-2203B,2204B,2204B-P1,2204B-P2,2205B, THE IZZZY-TENS (WL-2401), THE SLIM-TENS (WL-2402), THE MENS-TENS (WL2403), THE COMPACT TENS (WL-2302), DIGI-PRO TENS, MODEL WL-2204 AND WL-2205
6
Total
6
Cleared
0
Denied
FDA 510(k) Regulatory Record - Well-Life Healthcare, Inc. Physical Medicine ✕
1 devices