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MEDILAS D FAMILY LASERS

Page Type
Cleared 510(K)
510(k) Number
K070536
510(k) Type
Traditional
Applicant
DORNIER MEDTECH AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/21/2007
Days to Decision
84 days
Submission Type
Summary

MEDILAS D FAMILY LASERS

Page Type
Cleared 510(K)
510(k) Number
K070536
510(k) Type
Traditional
Applicant
DORNIER MEDTECH AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/21/2007
Days to Decision
84 days
Submission Type
Summary