HUMIDIFIER, ELECTRONIC (EH147)— 510(k) K760341

Name: FDA 510(k) clearance K760341
Creator: U.S. Food and Drug Administration
Published: 1976-08-11

Substantially Equivalent

Mistogen Equipment Co.

FDA 510(k) clearance K760341 for HUMIDIFIER, ELECTRONIC (EH147), Substantially Equivalent on 1976-08-11. Applicant: Mistogen Equipment Co.. Device class: 1.

Clearance details

Applicant: Mistogen Equipment Co.
Product code: Code KFZ
Device class: Class 1
Regulation: 21 CFR 868.5460
Advisory panel: Anesthesiology
Date received: 1976-07-30
Decision date: 1976-08-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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