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VIGGO VASCUPORT NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K881758
510(k) Type
Traditional
Applicant
OHMEDA MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/1988
Days to Decision
39 days

VIGGO VASCUPORT NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K881758
510(k) Type
Traditional
Applicant
OHMEDA MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/1988
Days to Decision
39 days