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VITAACCESS (TM) CATHETER INTRODUCER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K872998
510(k) Type
Traditional
Applicant
VITAPHORE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/1988
Days to Decision
234 days

VITAACCESS (TM) CATHETER INTRODUCER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K872998
510(k) Type
Traditional
Applicant
VITAPHORE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/1988
Days to Decision
234 days