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VITAACCESS CATHETER INTRODUCER KIT

Page Type
Cleared 510(K)
510(k) Number
K890435
510(k) Type
Traditional
Applicant
VITAPHORE CORP.
Country
United States
FDA Decision
Substantially Equivalent with Drug
Decision Date
3/29/1989
Days to Decision
61 days

VITAACCESS CATHETER INTRODUCER KIT

Page Type
Cleared 510(K)
510(k) Number
K890435
510(k) Type
Traditional
Applicant
VITAPHORE CORP.
Country
United States
FDA Decision
Substantially Equivalent with Drug
Decision Date
3/29/1989
Days to Decision
61 days