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VEINLASE, MODEL E50-K8-B5, SPECTRUM K8, MODEL E50-K8-B9

Page Type
Cleared 510(K)
510(k) Number
K000158
510(k) Type
Traditional
Applicant
FISMA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/2000
Days to Decision
218 days
Submission Type
Summary

VEINLASE, MODEL E50-K8-B5, SPECTRUM K8, MODEL E50-K8-B9

Page Type
Cleared 510(K)
510(k) Number
K000158
510(k) Type
Traditional
Applicant
FISMA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/2000
Days to Decision
218 days
Submission Type
Summary