Last synced on 20 December 2024 at 11:05 pm

RX HERCULINK 14 BILIARY STENT SYSTEM, MODELS 1005127-13, 1005129-13, 1005131-13, 1005133-13, 1005135-13, 1005137-13, 100

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001224
510(k) Type
Special
Applicant
GUIDANT CORP.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
5/17/2000
Days to Decision
30 days
Submission Type
Summary

RX HERCULINK 14 BILIARY STENT SYSTEM, MODELS 1005127-13, 1005129-13, 1005131-13, 1005133-13, 1005135-13, 1005137-13, 100

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001224
510(k) Type
Special
Applicant
GUIDANT CORP.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
5/17/2000
Days to Decision
30 days
Submission Type
Summary