CARDIOPHONE— 510(k) K894856

Substantially Equivalent

Euro-American Marketing Group, Inc.

FDA 510(k) clearance K894856 for CARDIOPHONE, Substantially Equivalent on 1990-01-18. Applicant: Euro-American Marketing Group, Inc..

Clearance details

Applicant: Euro-American Marketing Group, Inc.
Product code: Code DXH
Advisory panel: Cardiovascular
Date received: 1989-07-31
Decision date: 1990-01-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mount Prospect, IL, US

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