Last synced on 9 May 2025 at 11:05 pm

RX VIATRAC 14 PERIPHERAL DILATATION CATHETER, MODEL #'S 1003006-20, 1003007-20, 1003008-20, 1003009-20, 1003010-20, 1003

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K983055
510(k) Type
Traditional
Applicant
GUIDANT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/30/1998
Days to Decision
120 days
Submission Type
Summary

RX VIATRAC 14 PERIPHERAL DILATATION CATHETER, MODEL #'S 1003006-20, 1003007-20, 1003008-20, 1003009-20, 1003010-20, 1003

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K983055
510(k) Type
Traditional
Applicant
GUIDANT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/30/1998
Days to Decision
120 days
Submission Type
Summary