FDA 510(k) Applications Submitted by VAS-CATH, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K964881 12/05/1996 ULTRAVERSE PTA CATHETER VAS-CATH, INC.
K965178 12/24/1996 NIAGARA DUAL LUMEN CATHETER VAS-CATH, INC.
K973013 08/13/1997 OPTI-PLAST (CENTURION) 5.5F ANGIOPLASTY CATHETER VAS-CATH, INC.
K970725 02/28/1997 OPTI-PLAST XL 5.5 F PTA CATHETER VAS-CATH, INC.


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