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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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