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POWERLIPO LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K082096
510(k) Type
Traditional
Applicant
LUTRONIC CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/8/2008
Days to Decision
76 days
Submission Type
Summary

POWERLIPO LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K082096
510(k) Type
Traditional
Applicant
LUTRONIC CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/8/2008
Days to Decision
76 days
Submission Type
Summary