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VYGON SPLIT CANNULA INTRODUCER

Page Type
Cleared 510(K)
510(k) Number
K010913
510(k) Type
Traditional
Applicant
VYGON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/28/2001
Days to Decision
185 days
Submission Type
Statement

VYGON SPLIT CANNULA INTRODUCER

Page Type
Cleared 510(K)
510(k) Number
K010913
510(k) Type
Traditional
Applicant
VYGON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/28/2001
Days to Decision
185 days
Submission Type
Statement