The following data is part of a premarket notification filed by Usci, Div. C.r. Bard, Inc. with the FDA for Prosthesis, Vascular Bifurcated.
| Device ID | K760130 |
| 510k Number | K760130 |
| Device Name: | PROSTHESIS, VASCULAR BIFURCATED |
| Classification | Prosthesis, Vascular Graft, Of 6mm And Greater Diameter |
| Applicant | USCI, DIV. C.R. BARD, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DSY |
| CFR Regulation Number | 870.3450 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-06-28 |
| Decision Date | 1976-07-20 |