WM10, WM20, WM30 Power Massager

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K862041 ↗

FDA Product Code

ISA

Device Class

Class I

Regulation

21 CFR Part 890.5660

Advisory Committee

Physical Medicine

FDA Decision

SESE Substantially Equivalent

• BP800, 850 1000

  Class II

  FDA 510(k) K841095 Active Cleared 24 Aug 1984

• Foot Baths & Hand Massagers

  Class II

  FDA 510(k) K810034 Active Cleared 15 Jan 1981

• Whirlpool Aerator WB700, WB800, WB900, WB975

  Class II

  FDA 510(k) K872327 Active Cleared 4 Sep 1987

• Hp-20, 30, 40, 50 & 60

  Class II

  FDA 510(k) K841100 Active Cleared 23 Mar 1984

• SH20, SH30 & SH50 Ultrasonic Humidifier

  Class I

  FDA 510(k) K862042 Active Cleared 5 Jun 1986

• Pollenex Digital Thermometer T-225

  Class II

  FDA 510(k) K850363 Active Cleared 15 Feb 1985

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