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PROTEUS 235 PROTON THERAPY SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091629
510(k) Type
Traditional
Applicant
Ion Beam Applications S.A.
Country
Belgium
FDA Decision
Substantially Equivalent
Decision Date
8/11/2009
Days to Decision
69 days
Submission Type
Statement

PROTEUS 235 PROTON THERAPY SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091629
510(k) Type
Traditional
Applicant
Ion Beam Applications S.A.
Country
Belgium
FDA Decision
Substantially Equivalent
Decision Date
8/11/2009
Days to Decision
69 days
Submission Type
Statement