VisiRad XR— 510(k) K223133
Substantially EquivalentImidex, Inc.
FDA 510(k) clearance K223133 for VisiRad XR, Substantially Equivalent on 2023-08-03. Applicant: Imidex, Inc.. Device class: 2.
Clearance details
- Applicant
- Imidex, Inc.
- Product code
- Code MYN
- Device class
- Class 2
- Regulation
- 21 CFR 892.2070
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Denver, CO, US
Recent devices under product code MYN
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