FDA 510(k) Applications Submitted by IMPRA, INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K981076 |
03/24/1998 |
VENAFLO PTFE VASCULAR GRAFT, VENAFLO GRAFT WITH CARBON, VENAFLO VASCULAR GRAFT |
IMPRA, INC. |
K981079 |
03/24/1998 |
VENAFLO PTFE VASCULAR GRAFT, VENAFLO GRAFT WITH CARBON, VENAFLO VASCULAR GRAFT |
IMPRA, INC. |
K991027 |
03/29/1999 |
BI-DIRECTIONAL TUNNELER |
IMPRA, INC. |
K971192 |
03/31/1997 |
IMPRA EPTFE ARTERIOVENOUS CUFFED GRAFT |
IMPRA, INC. |
K983064 |
09/02/1998 |
IMPRA HIGH POROSITY GRAFT |
IMPRA, INC. |
K983769 |
10/26/1998 |
DISTAFLO BYPASS GRAFT |
IMPRA, INC. |
K983861 |
11/02/1998 |
DISTAFLO BYPASS GRAFT |
IMPRA, INC. |
K964877 |
12/05/1996 |
IMPRA EPTFE ARTERIOVENOUS CUFFED GRAFT |
IMPRA, INC. |
K004011 |
12/27/2000 |
IMPRA CARBOFLO VASCULAR GRAFT, IMPRA CARBOFLO VASCULAR GRAFTS FOR A-V ACCESS |
IMPRA, INC. |
K004012 |
12/27/2000 |
IMPRA CARBOFLO EPTFE VASCULAR GRAFTS |
IMPRA, INC. |
K962639 |
07/05/1996 |
IMPRA CARBOFLO EPTFE VASCULAR GRAFT |
IMPRA, INC. |
K964197 |
10/21/1996 |
IMPRA CARBOFLO EPTFE VASCULAR GRAFT |
IMPRA, INC. |
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