COMPUTER, CARDIAC OUTPUT, MODEL KM275— 510(k) K770675

Name: FDA 510(k) clearance K770675
Creator: U.S. Food and Drug Administration
Published: 1977-04-26

Substantially Equivalent

Lexington Instruments

FDA 510(k) clearance K770675 for COMPUTER, CARDIAC OUTPUT, MODEL KM275, Substantially Equivalent on 1977-04-26. Applicant: Lexington Instruments. Device class: 2.

Clearance details

Applicant: Lexington Instruments
Product code: Code DXG
Device class: Class 2
Regulation: 21 CFR 870.1435
Advisory panel: Cardiovascular
Date received: 1977-04-11
Decision date: 1977-04-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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