RADKOR, RF-159— 510(k) K883885
Substantially EquivalentRadkor, Inc.
FDA 510(k) clearance K883885 for RADKOR, RF-159, Substantially Equivalent on 1988-10-19. Applicant: Radkor, Inc.. Device class: 2.
Clearance details
- Applicant
- Radkor, Inc.
- Product code
- Code KXJ
- Device class
- Class 2
- Regulation
- 21 CFR 892.1980
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Irvine, CA, US
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