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MEGABEAM/CERALAS NON STERILE FIBER OPTIC LASER DELIVERY SYSTEMS, MODEL 200,320,400 OR 600UM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010689
510(k) Type
Traditional
Applicant
Biolitec, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/18/2001
Days to Decision
71 days
Submission Type
Summary

MEGABEAM/CERALAS NON STERILE FIBER OPTIC LASER DELIVERY SYSTEMS, MODEL 200,320,400 OR 600UM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010689
510(k) Type
Traditional
Applicant
Biolitec, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/18/2001
Days to Decision
71 days
Submission Type
Summary