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MULTIPULSE HOPLUS

Page Type
Cleared 510(K)
510(k) Number
K131987
510(k) Type
Traditional
Applicant
ASCLEPION LASER TECHNOLOGIES GMBH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
10/15/2014
Days to Decision
474 days
Submission Type
Summary

MULTIPULSE HOPLUS

Page Type
Cleared 510(K)
510(k) Number
K131987
510(k) Type
Traditional
Applicant
ASCLEPION LASER TECHNOLOGIES GMBH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
10/15/2014
Days to Decision
474 days
Submission Type
Summary