WH150 Room Humidifier

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K871661 ↗

FDA Product Code

KFZ

Device Class

Class I

Regulation

21 CFR Part 868.5460

Advisory Committee

Anesthesiology

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

• WM10, WM20, WM30 Power Massager

  Class I

  FDA 510(k) K862041 Active Cleared 17 Jun 1986

• SH20, SH30 & SH50 Ultrasonic Humidifier

  Class I

  FDA 510(k) K862042 Active Cleared 5 Jun 1986

See all devices from Associated Mills, Inc. →