MICRON ONE PORTA. ULTRASONIC NEBULIZER— 510(k) K850926

Name: FDA 510(k) clearance K850926
Creator: U.S. Food and Drug Administration
Published: 1985-05-23

Substantially Equivalent

Endotek Development Laboratories

FDA 510(k) clearance K850926 for MICRON ONE PORTA. ULTRASONIC NEBULIZER, Substantially Equivalent on 1985-05-23. Applicant: Endotek Development Laboratories. Device class: 1.

Clearance details

Applicant: Endotek Development Laboratories
Product code: Code CCQ
Device class: Class 1
Regulation: 21 CFR 868.5640
Advisory panel: Anesthesiology
Date received: 1985-03-05
Decision date: 1985-05-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

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