CARDIOPHONE— 510(k) K894856
Substantially EquivalentEuro-American Marketing Group, Inc.
FDA 510(k) clearance K894856 for CARDIOPHONE, Substantially Equivalent on 1990-01-18. Applicant: Euro-American Marketing Group, Inc.. Device class: 2.
Clearance details
- Applicant
- Euro-American Marketing Group, Inc.
- Product code
- Code DXH
- Device class
- Class 2
- Regulation
- 21 CFR 870.2920
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mount Prospect, IL, US
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