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Well-Life Healthcare, Inc.

FDA 510(k) & PMA Approved Devices — 6 products

Total Devices6
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K040512 LIMITED FUNCTION WL/OTC-TENS DEVICE, MODEL WL-2103A, WL-2203A, WL-2203B AND WL-2401GZJ2004-05-27 View
510(k) K033857 T-TECH DIGITAL, MODEL WL-22XXA SERIESGZJ2003-12-19 View
510(k) K030537 DIGI-PRO TENS/WL-2203B,2204B,2204B-P1,2204B-P2,2205BGZJ2003-03-20 View
510(k) K020020 THE IZZZY-TENS (WL-2401), THE SLIM-TENS (WL-2402), THE MENS-TENS (WL2403), THE COMPACT TENS (WL-2302)GZJ2002-12-30 View
510(k) K021359 DIGI-PRO TENS MODEL WL-2203 AND WL-2205GZJ2002-04-30 View
510(k) K020314 DIGI-PRO TENS, MODEL WL-2204 AND WL-2205IPF2002-04-30 View
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