SONIC MIST ULTRASONIC HUMIDIFIER— 510(k) K831646

Name: FDA 510(k) clearance K831646
Creator: U.S. Food and Drug Administration
Published: 1983-07-12

Substantially Equivalent

Douglas Products

FDA 510(k) clearance K831646 for SONIC MIST ULTRASONIC HUMIDIFIER, Substantially Equivalent on 1983-07-12. Applicant: Douglas Products. Device class: 1.

Clearance details

Applicant: Douglas Products
Product code: Code KFZ
Device class: Class 1
Regulation: 21 CFR 868.5460
Advisory panel: Anesthesiology
Date received: 1983-05-19
Decision date: 1983-07-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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Data sourced from openFDA. This site is unofficial and independent of the FDA.