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MEDIOSTAR XT

Page Type
Cleared 510(K)
510(k) Number
K050900
510(k) Type
Special
Applicant
ASCLEPION LASER TECHNOLOGIES GMBH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
5/16/2005
Days to Decision
35 days
Submission Type
Summary

MEDIOSTAR XT

Page Type
Cleared 510(K)
510(k) Number
K050900
510(k) Type
Special
Applicant
ASCLEPION LASER TECHNOLOGIES GMBH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
5/16/2005
Days to Decision
35 days
Submission Type
Summary