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MODIFIED LABEL TO PERCU. INTRO. W/SIDEPORT & 3-WAY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K894430
510(k) Type
Traditional
Applicant
DAIG CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/1989
Days to Decision
23 days

MODIFIED LABEL TO PERCU. INTRO. W/SIDEPORT & 3-WAY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K894430
510(k) Type
Traditional
Applicant
DAIG CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/1989
Days to Decision
23 days