Last synced on 25 April 2025 at 11:05 pm

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

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