The following data is part of a premarket notification filed by Exco, Inc. with the FDA for Vygon Stopcocks & Ramps(manifolds).
| Device ID | K813141 |
| 510k Number | K813141 |
| Device Name: | VYGON STOPCOCKS & RAMPS(MANIFOLDS) |
| Classification | Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass |
| Applicant | EXCO, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DTL |
| CFR Regulation Number | 870.4290 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-11-05 |
| Decision Date | 1981-11-27 |