QUIX DIGITAL RADIOGRAPHIC UPGRADE— 510(k) K052661
Substantially EquivalentEdge Medical Devices , Ltd.
FDA 510(k) clearance K052661 for QUIX DIGITAL RADIOGRAPHIC UPGRADE, Substantially Equivalent on 2006-06-07. Applicant: Edge Medical Devices , Ltd.. Device class: 2.
Clearance details
- Applicant
- Edge Medical Devices , Ltd.
- Product code
- Code MQB
- Device class
- Class 2
- Regulation
- 21 CFR 892.1680
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Raanana, IL
Recent devices under product code MQB
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