The following data is part of a premarket notification filed by Impra, Inc. with the FDA for Impra Eptfe Arteriovenous Cuffed Graft.
| Device ID | K964877 |
| 510k Number | K964877 |
| Device Name: | IMPRA EPTFE ARTERIOVENOUS CUFFED GRAFT |
| Classification | Prosthesis, Vascular Graft, Of Less Then 6mm Diameter |
| Applicant | IMPRA, INC. 1625 WEST 3RD ST. P.O. BOX 1740 Tempe, AZ 85281 |
| Contact | Kristi M Kistner |
| Correspondent | Kristi M Kistner IMPRA, INC. 1625 WEST 3RD ST. P.O. BOX 1740 Tempe, AZ 85281 |
| Product Code | DYF |
| CFR Regulation Number | 870.3450 [🔎] |
| Decision | Se Subject To Tracking Reg (ST) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-12-05 |
| Decision Date | 1997-03-20 |
| Summary: | summary |