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HIGH-DEFINITION 120 MULTILEAF COLLIMATOR (HD120 MLC)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071992
510(k) Type
Special
Applicant
Varian Medical Systems
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/2007
Days to Decision
26 days
Submission Type
Summary

HIGH-DEFINITION 120 MULTILEAF COLLIMATOR (HD120 MLC)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071992
510(k) Type
Special
Applicant
Varian Medical Systems
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/2007
Days to Decision
26 days
Submission Type
Summary