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PINPOINTE FOOTLASER MODEL 6W, 30W, 100W

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093545
510(k) Type
Traditional
Applicant
INCISIVE, INC. (FORMERLY NAMED INCISIVE, LLC)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/15/2010
Days to Decision
332 days
Submission Type
Summary

PINPOINTE FOOTLASER MODEL 6W, 30W, 100W

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093545
510(k) Type
Traditional
Applicant
INCISIVE, INC. (FORMERLY NAMED INCISIVE, LLC)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/15/2010
Days to Decision
332 days
Submission Type
Summary