FUSION DIGITAL DIAGNOSTIC X-RAY UPGRADE KIT— 510(k) K141743
Substantially EquivalentRadiology Solutions, LLC
FDA 510(k) clearance K141743 for FUSION DIGITAL DIAGNOSTIC X-RAY UPGRADE KIT, Substantially Equivalent on 2014-10-03. Applicant: Radiology Solutions, LLC. Device class: 2.
Clearance details
- Applicant
- Radiology Solutions, LLC
- 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
- Naples, FL, US
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