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DORNIER DIODE LASER FAMILY MEDILAS D, MEDILAS D SKINPULSE & MEDILAS D SKINPULSE S LASER SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020339
510(k) Type
Traditional
Applicant
Dornier Medtech America, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/25/2002
Days to Decision
266 days
Submission Type
Summary

DORNIER DIODE LASER FAMILY MEDILAS D, MEDILAS D SKINPULSE & MEDILAS D SKINPULSE S LASER SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020339
510(k) Type
Traditional
Applicant
Dornier Medtech America, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/25/2002
Days to Decision
266 days
Submission Type
Summary