MINI OX III OXYGEN MONITOR— 510(k) K833326

Name: FDA 510(k) clearance K833326
Creator: U.S. Food and Drug Administration
Published: 1983-11-03

Substantially Equivalent

Catalyst Research Corp.

FDA 510(k) clearance K833326 for MINI OX III OXYGEN MONITOR, Substantially Equivalent on 1983-11-03. Applicant: Catalyst Research Corp.. Device class: 1.

Clearance details

Applicant: Catalyst Research Corp.
Product code: Code BXL
Device class: Class 1
Regulation: 21 CFR 868.1030
Advisory panel: Anesthesiology
Date received: 1983-09-27
Decision date: 1983-11-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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