Last synced on 14 November 2025 at 11:06 pm

VYGON XRO VENOUS/ARTERIAL UMBILICAL CATHETER

Page Type
Cleared 510(K)
510(k) Number
K921374
510(k) Type
Traditional
Applicant
VYGON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/1992
Days to Decision
221 days
Submission Type
Statement

VYGON XRO VENOUS/ARTERIAL UMBILICAL CATHETER

Page Type
Cleared 510(K)
510(k) Number
K921374
510(k) Type
Traditional
Applicant
VYGON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/1992
Days to Decision
221 days
Submission Type
Statement