The following data is part of a premarket notification filed by Renal Systems, Inc. with the FDA for Hemasite Accessories Modification.
| Device ID | K840437 |
| 510k Number | K840437 |
| Device Name: | HEMASITE ACCESSORIES MODIFICATION |
| Classification | Accessories, A-v Shunt |
| Applicant | RENAL SYSTEMS, 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 | 1984-02-01 |
| Decision Date | 1984-02-21 |