CARDIOCAP II CG-2GS, 2G, 1GS, 1G, 2CG, CS MONITOR— 510(k) K902493

Name: FDA 510(k) clearance K902493
Creator: U.S. Food and Drug Administration
Published: 1990-07-06

Substantially Equivalent

Datex Division Instrumentarium Corp.

FDA 510(k) clearance K902493 for CARDIOCAP II CG-2GS, 2G, 1GS, 1G, 2CG, CS MONITOR, Substantially Equivalent on 1990-07-06. Applicant: Datex Division Instrumentarium Corp.. Device class: 1.

Clearance details

Applicant: Datex Division Instrumentarium Corp.
Product code: Code DRI
Device class: Class 1
Regulation: 21 CFR 870.2620
Advisory panel: Cardiovascular
Date received: 1990-06-05
Decision date: 1990-07-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Helsinki, Finland, FI

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