ARTERIAL BLOOD GAS INTERPRETATION PROG— 510(k) K840102

Name: FDA 510(k) clearance K840102
Creator: U.S. Food and Drug Administration
Published: 1984-02-04

Substantially Equivalent

M. D. Software, Inc.

FDA 510(k) clearance K840102 for ARTERIAL BLOOD GAS INTERPRETATION PROG, Substantially Equivalent on 1984-02-04. Applicant: M. D. Software, Inc.. Device class: 2.

Clearance details

Applicant: M. D. Software, Inc.
Product code: Code CCE
Device class: Class 2
Regulation: 21 CFR 868.1200
Advisory panel: Anesthesiology
Date received: 1984-01-10
Decision date: 1984-02-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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