Whirlpool Aerator WB700, WB800, WB900, WB975

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K872327 ↗

FDA Product Code

ILJ

Device Class

Class II

Regulation

21 CFR Part 890.5100

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

• 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

• Pollenex Digital Thermometer T-225

  Class II

  FDA 510(k) K850363 Active Cleared 15 Feb 1985

See all devices from Associated Mills, Inc. →

• What is the purpose of the Whirlpool Aerator?

  The Whirlpool Aerator is designed to generate aerated water for whirlpool baths, providing hydro-massage therapy to relieve aching and sore muscles in clinical or home-based physical therapy settings.

• Is the Whirlpool Aerator single-use or reusable?

  The Whirlpool Aerator is listed as a single-use or disposable component in some configurations, though specific reuse instructions are not detailed in the available documentation.

• What models of the Whirlpool Aerator are available?

  The Whirlpool Aerator is available in models WB700, WB800, WB900, and WB975, all designed to generate aerated water for whirlpool baths providing hydro-massage therapy.

• What is the regulatory classification of this device?

  The Whirlpool Aerator is classified under product code ILJ and device class 2, with FDA 510(k) clearance granted under K872327 on September 4, 1987, for use in physical medicine applications.