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ENDOVASCULAR LAER VEIN SYSTEM KIT

Page Type
Cleared 510(K)
510(k) Number
K101712
510(k) Type
Traditional
Applicant
BIOLITEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/27/2010
Days to Decision
131 days
Submission Type
Summary

ENDOVASCULAR LAER VEIN SYSTEM KIT

Page Type
Cleared 510(K)
510(k) Number
K101712
510(k) Type
Traditional
Applicant
BIOLITEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/27/2010
Days to Decision
131 days
Submission Type
Summary