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PROFILE 1064 LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K023881
510(k) Type
Traditional
Applicant
SCITON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/13/2003
Days to Decision
204 days
Submission Type
Summary

PROFILE 1064 LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K023881
510(k) Type
Traditional
Applicant
SCITON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/13/2003
Days to Decision
204 days
Submission Type
Summary