SH20, SH30 & SH50 Ultrasonic Humidifier

FDA 510(k) K862042 · Associated Mills, Inc.

Substantially Equivalent

510(k) numberK862042

Submission

Device name
SH20, SH30 & SH50 Ultrasonic Humidifier
Applicant
Associated Mills, Inc.
Chicago, IL, US
Received
May 28, 1986
Decision date
June 5, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KFZ – Humidifier, Non-Direct Patient Interface (Home-Use)
Device class
Class I (low risk)
Regulation
21 CFR 868.5460
Specialty
Anesthesiology

Other 510(k)s with product code KFZ

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K950116Therasteam Personal Steam InhalerKFZ · Traditional Kaz, Inc.02/10/1995SE
K915603Virotherm HumidifierKFZ · Traditional Virotherm Laboratory10/22/1992SE
K894734Rhinotherm Ultra 2KFZ · Traditional Twinmed Products, Inc.02/16/1990SE
K871661WH150 Room HumidifierKFZ · Traditional Associated Mills, Inc.06/15/1987SE
K871189Sunbeam Dura-Vap Warm Steam Vaporizer Model 1380KFZ · Traditional Sunbeam Appliance Service Co.05/08/1987SE
K862919Transpirator(Tm) MT-1000 Personal HumidifierKFZ · Traditional Transpirator Technologics, Inc.11/07/1986SE
K862171MP-500 Electronic NebulizerKFZ · Traditional The Timeter Group07/14/1986SE
K851220Sunbeam Evaporative Humidifier 663 & 664KFZ · Traditional Northern Electric Co. Div. of Sunbeam Corp.09/17/1985SE
K852283Thermix Inc. Nasotherm II Personal Steam MachineKFZ · Traditional Thermix, Inc.07/30/1985SE
K850711Inhalation Therapy Nebulizer DeviceKFZ · Traditional Med USA06/05/1985SE

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K871661WH150 Room HumidifierKFZ · Traditional 06/15/1987SE
K862041WM10, WM20, WM30 Power MassagerISA · Traditional 06/17/1986SE
K844397Pollenex Digital Sphygmomanometer BP-4000DSK · Traditional 04/18/1985SE
K844396Pollenex Digital Sphygmomanometer BP-2000DSK · Traditional 04/18/1985SE
K850363Pollenex Digital Thermometer T-225FLL · Traditional 02/15/1985SE
K850362Pollenex Digital Thermometer T-125FLL · Traditional 02/15/1985SE
K841095BP800, 850 1000DXN · Traditional 08/24/1984SE
K841100HP-20, 30, 40, 50 & 60IRT · Traditional 03/23/1984SE

Questions and answers

When was SH20, SH30 & SH50 Ultrasonic Humidifier cleared by the FDA?

SH20, SH30 & SH50 Ultrasonic Humidifier (K862042) received a 510(k) decision of Substantially Equivalent on June 5, 1986, 8 days after the submission was received.

What is the product code of K862042?

The FDA product code is KFZ – Humidifier, Non-Direct Patient Interface (Home-Use), a Class I (low risk) device regulated under 21 CFR 868.5460.