Last synced on 18 April 2025 at 11:05 pm

ATW MARKER WIRE STEERABLE GUIDEWIRE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K994358
510(k) Type
Special
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/13/2000
Days to Decision
17 days
Submission Type
Summary

ATW MARKER WIRE STEERABLE GUIDEWIRE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K994358
510(k) Type
Special
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/13/2000
Days to Decision
17 days
Submission Type
Summary