Last synced on 18 April 2025 at 11:05 pm

ACS HI-TORQUE CROSS-IT 400XT GUIDE WIRE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992169
510(k) Type
Traditional
Applicant
ADVANCED CARDIOVASCULAR SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/28/1999
Days to Decision
122 days
Submission Type
Summary

ACS HI-TORQUE CROSS-IT 400XT GUIDE WIRE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992169
510(k) Type
Traditional
Applicant
ADVANCED CARDIOVASCULAR SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/28/1999
Days to Decision
122 days
Submission Type
Summary