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CERALAS D 10-60 810NM LASER SYSTEM WITH ENDO LASER VEIN SYSTEM KIT

Page Type
Cleared 510(K)
510(k) Number
K030700
510(k) Type
Traditional
Applicant
BIOLITEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/4/2003
Days to Decision
90 days
Submission Type
Summary

CERALAS D 10-60 810NM LASER SYSTEM WITH ENDO LASER VEIN SYSTEM KIT

Page Type
Cleared 510(K)
510(k) Number
K030700
510(k) Type
Traditional
Applicant
BIOLITEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/4/2003
Days to Decision
90 days
Submission Type
Summary