CADPLAN HELIOS OPTION 6.0— 510(k) K984532
Substantially EquivalentVarian Medical Systems, Inc.
FDA 510(k) clearance K984532 for CADPLAN HELIOS OPTION 6.0, Substantially Equivalent on 1999-08-09. Applicant: Varian Medical Systems, Inc.. Device class: 2.
Clearance details
- Applicant
- Varian Medical Systems, Inc.
- Product code
- Code MUJ
- 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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