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MULTICATH EXPERT

Page Type
Cleared 510(K)
510(k) Number
K061250
510(k) Type
Traditional
Applicant
VYGON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/2006
Days to Decision
148 days
Submission Type
Summary

MULTICATH EXPERT

Page Type
Cleared 510(K)
510(k) Number
K061250
510(k) Type
Traditional
Applicant
VYGON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/2006
Days to Decision
148 days
Submission Type
Summary