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PROFILE 1320 LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K022381
510(k) Type
Traditional
Applicant
SCITON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/2002
Days to Decision
88 days
Submission Type
Summary

PROFILE 1320 LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K022381
510(k) Type
Traditional
Applicant
SCITON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/2002
Days to Decision
88 days
Submission Type
Summary