ProBeam 360° Proton Therapy System— 510(k) K221791
Substantially EquivalentVarian Medical Systems, Inc.
FDA 510(k) clearance K221791 for ProBeam 360° Proton Therapy System, Substantially Equivalent on 2022-12-01. Applicant: Varian Medical Systems, Inc.. Device class: 2.
Clearance details
- Applicant
- Varian Medical Systems, Inc.
- Product code
- Code LHN
- Device class
- Class 2
- Regulation
- 21 CFR 892.5050
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Palo Alto, CA, US
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