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PERCUTANEOUS INTROD W/SIDEPORT/THREE-WAY STOPCOCK

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K910861
510(k) Type
Traditional
Applicant
DAIG CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/7/1991
Days to Decision
81 days

PERCUTANEOUS INTROD W/SIDEPORT/THREE-WAY STOPCOCK

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K910861
510(k) Type
Traditional
Applicant
DAIG CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/7/1991
Days to Decision
81 days