Well-Life Healthcare, Inc.
Well-Life Healthcare, Inc. holds FDA 510(k) medical device clearances, first cleared 2002, most recent 2004.
Top product codes for Well-Life Healthcare, Inc.
Recent clearances by Well-Life Healthcare, Inc.
- K040512 — LIMITED FUNCTION WL/OTC-TENS DEVICE, MODEL WL-2103A, WL-2203A, WL-2203B AND WL-2401
- K033857 — T-TECH DIGITAL, MODEL WL-22XXA SERIES
- K030537 — DIGI-PRO TENS/WL-2203B,2204B,2204B-P1,2204B-P2,2205B
- K020020 — THE IZZZY-TENS (WL-2401), THE SLIM-TENS (WL-2402), THE MENS-TENS (WL2403), THE COMPACT TENS (WL-2302)
- K020314 — DIGI-PRO TENS, MODEL WL-2204 AND WL-2205
- K021359 — DIGI-PRO TENS MODEL WL-2203 AND WL-2205
Data sourced from openFDA. This site is unofficial and independent of the FDA.