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

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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