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VARICES NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K031238
510(k) Type
Traditional
Applicant
SCANDIMED. A.S.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/4/2004
Days to Decision
535 days
Submission Type
Statement

VARICES NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K031238
510(k) Type
Traditional
Applicant
SCANDIMED. A.S.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/4/2004
Days to Decision
535 days
Submission Type
Statement