TRAVENOL ULTRASONIC NEBULIZER CUPS— 510(k) K802054

Name: FDA 510(k) clearance K802054
Creator: U.S. Food and Drug Administration
Published: 1980-12-01

Substantially Equivalent

Travenol Laboratories, S.A.

FDA 510(k) clearance K802054 for TRAVENOL ULTRASONIC NEBULIZER CUPS, Substantially Equivalent on 1980-12-01. Applicant: Travenol Laboratories, S.A.. Device class: 2.

Clearance details

Applicant: Travenol Laboratories, S.A.
Product code: Code CAP
Device class: Class 2
Regulation: 21 CFR 868.2600
Advisory panel: Anesthesiology
Date received: 1980-08-25
Decision date: 1980-12-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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