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ONCENTRA, ONCENTRA EXTERNAL BEAM, ONCENTRA BRACHY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121448
510(k) Type
Traditional
Applicant
ELEKTA INC. D/B/A NUCLETRON CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/2/2012
Days to Decision
48 days
Submission Type
Summary

ONCENTRA, ONCENTRA EXTERNAL BEAM, ONCENTRA BRACHY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121448
510(k) Type
Traditional
Applicant
ELEKTA INC. D/B/A NUCLETRON CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/2/2012
Days to Decision
48 days
Submission Type
Summary