Last synced on 30 May 2025 at 11:05 pm

INSYTE, ANGIOCATH, INSYTE AUTOGUARD, ANGIOCATH AUTOGUARD, AUTOGUARD PRO, INTIMA, AND SAF-T-INTIMA INTRAVASCULAR CATHETE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013800
510(k) Type
Traditional
Applicant
BECTON DICKINSON INFUSION THERAPY SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/2001
Days to Decision
36 days
Submission Type
Summary

INSYTE, ANGIOCATH, INSYTE AUTOGUARD, ANGIOCATH AUTOGUARD, AUTOGUARD PRO, INTIMA, AND SAF-T-INTIMA INTRAVASCULAR CATHETE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013800
510(k) Type
Traditional
Applicant
BECTON DICKINSON INFUSION THERAPY SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/2001
Days to Decision
36 days
Submission Type
Summary