The following data is part of a premarket notification filed by D/p, Inc. with the FDA for Vein Graft Cannula.
| Device ID | K791832 |
| 510k Number | K791832 |
| Device Name: | VEIN GRAFT CANNULA |
| Classification | Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass |
| Applicant | D/P, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DWF |
| CFR Regulation Number | 870.4210 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-09-18 |
| Decision Date | 1979-10-04 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 20613994926771 | K791832 | 000 |
| 20613994926757 | K791832 | 000 |
| 10889942055203 | K791832 | 000 |