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DORNIER DIODE LASER FAMILY, INCLUDING MEDILAS D FIBERTOM, MEDILAS D SKINPULSE & MEDILAS D SKINPULSE S LASER SYSTEMS

Page Type
Cleared 510(K)
510(k) Number
K021724
510(k) Type
Traditional
Applicant
DORNIER MEDTECH AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/19/2002
Days to Decision
87 days
Submission Type
Summary

DORNIER DIODE LASER FAMILY, INCLUDING MEDILAS D FIBERTOM, MEDILAS D SKINPULSE & MEDILAS D SKINPULSE S LASER SYSTEMS

Page Type
Cleared 510(K)
510(k) Number
K021724
510(k) Type
Traditional
Applicant
DORNIER MEDTECH AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/19/2002
Days to Decision
87 days
Submission Type
Summary