Last synced on 25 January 2026 at 3:41 am

CVD SMALL VESSEL BALLOON DILATION CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K942150
510(k) Type
Traditional
Applicant
CARDIO-DYNAMICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/1994
Days to Decision
91 days
Submission Type
Summary

CVD SMALL VESSEL BALLOON DILATION CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K942150
510(k) Type
Traditional
Applicant
CARDIO-DYNAMICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/1994
Days to Decision
91 days
Submission Type
Summary