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MODEIFICATION TO IPLAN RT DOSE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080888
510(k) Type
Special
Applicant
BRAINLAB AG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
6/11/2008
Days to Decision
72 days
Submission Type
Summary

MODEIFICATION TO IPLAN RT DOSE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080888
510(k) Type
Special
Applicant
BRAINLAB AG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
6/11/2008
Days to Decision
72 days
Submission Type
Summary