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CERALAS D10-60 810NM DIODE LASER, MODELCERALAS DIO-60

Page Type
Cleared 510(K)
510(k) Number
K020835
510(k) Type
Traditional
Applicant
BIOLITEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/12/2002
Days to Decision
90 days
Submission Type
Summary

CERALAS D10-60 810NM DIODE LASER, MODELCERALAS DIO-60

Page Type
Cleared 510(K)
510(k) Number
K020835
510(k) Type
Traditional
Applicant
BIOLITEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/12/2002
Days to Decision
90 days
Submission Type
Summary