COBRASCAN CX-312— 510(k) K953942
Substantially EquivalentRadiographic Digital Imaging, Inc.
FDA 510(k) clearance K953942 for COBRASCAN CX-312, Substantially Equivalent on 1995-12-22. Applicant: Radiographic Digital Imaging, Inc.. Device class: 2.
Clearance details
- Applicant
- Radiographic Digital Imaging, Inc.
- Product code
- Code LMA
- Device class
- Class 2
- Regulation
- 21 CFR 892.2030
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Compton, CA, US
Recent devices under product code LMA
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