Precision Treatment Planning System— 510(k) K161136
Substantially EquivalentAccuray Incorporated
FDA 510(k) clearance K161136 for Precision Treatment Planning System, Substantially Equivalent on 2016-06-24. Applicant: Accuray Incorporated. Device class: 2.
Clearance details
- Applicant
- Accuray Incorporated
- 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
- Sunnyvale, CA, US
Recent devices under product code MUJ
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- K171837 — TomoTherapy Treatment Delivery System with iDMS
Data sourced from openFDA. This site is unofficial and independent of the FDA.