G.E. DXS 350/550/650/650II SINGLE PHASE GENERATORS— 510(k) K902987
Substantially EquivalentElectromek Diagnostic Systems, Inc.
FDA 510(k) clearance K902987 for G.E. DXS 350/550/650/650II SINGLE PHASE GENERATORS, Substantially Equivalent on 1990-12-26. Applicant: Electromek Diagnostic Systems, Inc.. Device class: 1.
Clearance details
- Applicant
- Electromek Diagnostic Systems, Inc.
- Product code
- Code IZO
- Device class
- Class 1
- Regulation
- 21 CFR 892.1700
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Troy, IL, US
Recent devices under product code IZO
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