RADKOR DXG-650R— 510(k) K895969
Substantially EquivalentRadkor, Inc.
FDA 510(k) clearance K895969 for RADKOR DXG-650R, Substantially Equivalent on 1989-11-13. Applicant: Radkor, Inc.. Device class: 1.
Clearance details
- Applicant
- Radkor, Inc.
- Product code
- Code IZO
- Device class
- Class 1
- Regulation
- 21 CFR 892.1700
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Irvine, CA, US
Recent devices under product code IZO
view allMore clearances from Radkor, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.