CM5000R REMOTE INDICATOR— 510(k) K931394

Name: FDA 510(k) clearance K931394
Creator: U.S. Food and Drug Administration
Published: 1993-07-01

Substantially Equivalent

Canadian Monaghan , Ltd.

FDA 510(k) clearance K931394 for CM5000R REMOTE INDICATOR, Substantially Equivalent on 1993-07-01. Applicant: Canadian Monaghan , Ltd.. Device class: 2.

Clearance details

Applicant: Canadian Monaghan , Ltd.
Product code: Code CAP
Device class: Class 2
Regulation: 21 CFR 868.2600
Advisory panel: Anesthesiology
Date received: 1993-03-19
Decision date: 1993-07-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: London, Ontario, CA

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.