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SURECAUT DIAMOND LASER KNIFE

Page Type
Cleared 510(K)
510(k) Number
K983463
510(k) Type
Traditional
Applicant
CLINICON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/11/1998
Days to Decision
71 days
Submission Type
Summary

SURECAUT DIAMOND LASER KNIFE

Page Type
Cleared 510(K)
510(k) Number
K983463
510(k) Type
Traditional
Applicant
CLINICON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/11/1998
Days to Decision
71 days
Submission Type
Summary