The following data is part of a premarket notification filed by Intervascular, Inc. with the FDA for Lp200 & Hp800 Series Vascular Prosth.
| Device ID | K833716 |
| 510k Number | K833716 |
| Device Name: | LP200 & HP800 SERIES VASCULAR PROSTH |
| Classification | Prosthesis, Vascular Graft, Of 6mm And Greater Diameter |
| Applicant | INTERVASCULAR, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | DSY |
| CFR Regulation Number | 870.3450 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-10-21 |
| Decision Date | 1984-01-10 |