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DORNIER MEDILAS D LITEBEAM+ 1470

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110364
510(k) Type
Traditional
Applicant
Dornier Medtech America, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/7/2011
Days to Decision
303 days
Submission Type
Summary

DORNIER MEDILAS D LITEBEAM+ 1470

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110364
510(k) Type
Traditional
Applicant
Dornier Medtech America, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/7/2011
Days to Decision
303 days
Submission Type
Summary