PVMED DDR 2520 DIGITAL IMAGING SYSTEM— 510(k) K072766
Substantially EquivalentPortavision Medical
FDA 510(k) clearance K072766 for PVMED DDR 2520 DIGITAL IMAGING SYSTEM, Substantially Equivalent on 2007-12-11. Applicant: Portavision Medical. Device class: 2.
Clearance details
- Applicant
- Portavision Medical
- Product code
- Code IXK
- Device class
- Class 2
- Regulation
- 21 CFR 892.1630
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Austin, TX, US
Recent devices under product code IXK
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