Last synced on 25 January 2026 at 3:41 am

OPTI-PLAST ANGIOPLASTY CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K941706
510(k) Type
Traditional
Applicant
VAS-CATH, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
10/18/1994
Days to Decision
195 days
Submission Type
Statement

OPTI-PLAST ANGIOPLASTY CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K941706
510(k) Type
Traditional
Applicant
VAS-CATH, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
10/18/1994
Days to Decision
195 days
Submission Type
Statement