The following data is part of a premarket notification filed by Advocacy International, Ltd. with the FDA for Asahi Hollow Fiber Kidneys, Am-series.
| Device ID | K830231 |
| 510k Number | K830231 |
| Device Name: | ASAHI HOLLOW FIBER KIDNEYS, AM-SERIES |
| Classification | Accessories, Blood Circuit, Hemodialysis |
| Applicant | ADVOCACY INTERNATIONAL, LTD. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KOC |
| CFR Regulation Number | 876.5820 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-01-18 |
| Decision Date | 1983-03-17 |