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NES REPROCESSED VARICOSE VEIN RF CATHETER

Page Type
Cleared 510(K)
510(k) Number
K090661
510(k) Type
Traditional
Applicant
Northeast Scientific, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/21/2010
Days to Decision
496 days
Submission Type
Summary

NES REPROCESSED VARICOSE VEIN RF CATHETER

Page Type
Cleared 510(K)
510(k) Number
K090661
510(k) Type
Traditional
Applicant
Northeast Scientific, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/21/2010
Days to Decision
496 days
Submission Type
Summary