CM 3000 THE MONITOR— 510(k) K874898

Name: FDA 510(k) clearance K874898
Creator: U.S. Food and Drug Administration
Published: 1988-03-21

Substantially Equivalent

Lifeline Medical Systems, Inc.

FDA 510(k) clearance K874898 for CM 3000 THE MONITOR, Substantially Equivalent on 1988-03-21. Applicant: Lifeline Medical Systems, Inc.. Device class: 2.

Clearance details

Applicant: Lifeline Medical Systems, Inc.
Product code: Code BZQ
Device class: Class 2
Regulation: 21 CFR 868.2375
Advisory panel: Anesthesiology
Date received: 1987-12-01
Decision date: 1988-03-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tualatin, OR, US

Download summary PDF View on FDA.gov ↗

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