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ACCUSCULPT II LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K101573
510(k) Type
Traditional
Applicant
LUTRONIC CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/23/2010
Days to Decision
108 days
Submission Type
Summary

ACCUSCULPT II LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K101573
510(k) Type
Traditional
Applicant
LUTRONIC CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/23/2010
Days to Decision
108 days
Submission Type
Summary