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LIGHTLANCE LASER SKIN PERFORATOR

Page Type
Cleared 510(K)
510(k) Number
K013021
510(k) Type
Traditional
Applicant
INNOTECH USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/30/2002
Days to Decision
265 days
Submission Type
Summary

LIGHTLANCE LASER SKIN PERFORATOR

Page Type
Cleared 510(K)
510(k) Number
K013021
510(k) Type
Traditional
Applicant
INNOTECH USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/30/2002
Days to Decision
265 days
Submission Type
Summary