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MEVION S250i Proton Beam Radiation Therapy Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172848
510(k) Type
Traditional
Applicant
Mevion Medical Systems
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/27/2017
Days to Decision
99 days
Submission Type
Summary

MEVION S250i Proton Beam Radiation Therapy Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172848
510(k) Type
Traditional
Applicant
Mevion Medical Systems
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/27/2017
Days to Decision
99 days
Submission Type
Summary