GAMMAMED 212 AND 232 SOURCE ASSEMBLY— 510(k) K030745
Substantially EquivalentVarian Medical Systems
FDA 510(k) clearance K030745 for GAMMAMED 212 AND 232 SOURCE ASSEMBLY, Substantially Equivalent on 2003-03-12. Applicant: Varian Medical Systems. Device class: 2.
Clearance details
- Applicant
- Varian Medical Systems
- Product code
- Code KXK
- Device class
- Class 2
- Regulation
- 21 CFR 892.5730
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Charlottesville, VA, US
Recent devices under product code KXK
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