Last synced on 25 April 2025 at 11:05 pm

MEDILAS D FAMILY LASERS, INCLUDING MEDILAS D LITEBEAM, LITEBEAM +, UROBEAM, MULTIBEAM, FLEXIPULSE AND MAGNAPULSE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K083258
510(k) Type
Traditional
Applicant
DORNIER MEDTECH AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/2009
Days to Decision
87 days
Submission Type
Summary

MEDILAS D FAMILY LASERS, INCLUDING MEDILAS D LITEBEAM, LITEBEAM +, UROBEAM, MULTIBEAM, FLEXIPULSE AND MAGNAPULSE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K083258
510(k) Type
Traditional
Applicant
DORNIER MEDTECH AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/2009
Days to Decision
87 days
Submission Type
Summary