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SUREGUIDE CO2 LASER BEAM DELIVERY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K992472
510(k) Type
Traditional
Applicant
CLINICON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/8/1999
Days to Decision
44 days
Submission Type
Summary

SUREGUIDE CO2 LASER BEAM DELIVERY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K992472
510(k) Type
Traditional
Applicant
CLINICON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/8/1999
Days to Decision
44 days
Submission Type
Summary