ARGIS PULMONARY FUNCTION TESTING SYSTEM— 510(k) K921306

Name: FDA 510(k) clearance K921306
Creator: U.S. Food and Drug Administration
Published: 1993-06-25

Substantially Equivalent

Med Science

FDA 510(k) clearance K921306 for ARGIS PULMONARY FUNCTION TESTING SYSTEM, Substantially Equivalent on 1993-06-25. Applicant: Med Science. Device class: 2.

Clearance details

Applicant: Med Science
Product code: Code BZC
Device class: Class 2
Regulation: 21 CFR 868.1880
Advisory panel: Anesthesiology
Date received: 1992-03-18
Decision date: 1993-06-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jacksonville, FL, US

Download summary PDF View on FDA.gov ↗

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