FAXITRON DIGITAL RADIOGRAPHY SYSTEM, MODEL DX-50— 510(k) K061361
Substantially EquivalentFaxitron X-Ray Corp.
FDA 510(k) clearance K061361 for FAXITRON DIGITAL RADIOGRAPHY SYSTEM, MODEL DX-50, Substantially Equivalent on 2006-08-15. Applicant: Faxitron X-Ray Corp.. Device class: 2.
Clearance details
- Applicant
- Faxitron X-Ray Corp.
- Product code
- Code MWP
- Device class
- Class 2
- Regulation
- 21 CFR 892.1680
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Wheeling, IL, US
Recent devices under product code MWP
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