PVMED DDR 2430T— 510(k) K133524
Substantially EquivalentPortavision Medical, LLC
FDA 510(k) clearance K133524 for PVMED DDR 2430T, Substantially Equivalent on 2014-04-16. Applicant: Portavision Medical, LLC. Device class: 2.
Clearance details
- Applicant
- Portavision Medical, 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
- Kenner, LA, US
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