G.E. MONITROL 90 AND G.E. MONITROL 15— 510(k) K902989
Substantially EquivalentElectromek Diagnostic Systems, Inc.
FDA 510(k) clearance K902989 for G.E. MONITROL 90 AND G.E. MONITROL 15, Substantially Equivalent on 1990-10-29. Applicant: Electromek Diagnostic Systems, Inc.. Device class: 2.
Clearance details
- Applicant
- Electromek Diagnostic Systems, Inc.
- Product code
- Code IXR
- Device class
- Class 2
- Regulation
- 21 CFR 892.1980
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Troy, IL, US
Recent devices under product code IXR
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