ULTRASONIC HUMIDIFIER— 510(k) K790966

Name: FDA 510(k) clearance K790966
Creator: U.S. Food and Drug Administration
Published: 1979-06-11

Substantially Equivalent

Hankscraft Div. of Gerber Products Co.

FDA 510(k) clearance K790966 for ULTRASONIC HUMIDIFIER, Substantially Equivalent on 1979-06-11. Applicant: Hankscraft Div. of Gerber Products Co.. Device class: 1.

Clearance details

Applicant: Hankscraft Div. of Gerber Products Co.
Product code: Code KFZ
Device class: Class 1
Regulation: 21 CFR 868.5460
Advisory panel: Anesthesiology
Date received: 1979-05-22
Decision date: 1979-06-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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