The following data is part of a premarket notification filed by Medical Components, Inc. with the FDA for Double Lumen Sublcavian-femoral.
| Device ID | K841530 |
| 510k Number | K841530 |
| Device Name: | DOUBLE LUMEN SUBLCAVIAN-FEMORAL |
| Classification | Accessories, A-v Shunt |
| Applicant | MEDICAL COMPONENTS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KNZ |
| CFR Regulation Number | 876.5540 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-04-03 |
| Decision Date | 1984-06-25 |