RECOMED CARDIAC OUTPUT METER 236067-— 510(k) K840439

Name: FDA 510(k) clearance K840439
Creator: U.S. Food and Drug Administration
Published: 1984-11-20

Substantially Equivalent

Litton Medical Electronics

FDA 510(k) clearance K840439 for RECOMED CARDIAC OUTPUT METER 236067-, Substantially Equivalent on 1984-11-20. Applicant: Litton Medical Electronics. Device class: 2.

Clearance details

Applicant: Litton Medical Electronics
Product code: Code DXG
Device class: Class 2
Regulation: 21 CFR 870.1435
Advisory panel: Cardiovascular
Date received: 1984-02-01
Decision date: 1984-11-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Elk Grove Village, IL, US

Download summary PDF View on FDA.gov ↗

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