The following data is part of a premarket notification filed by Millipore Corp. with the FDA for Kpp Peritoneal Dialysate Filter.
| Device ID | K803275 |
| 510k Number | K803275 |
| Device Name: | KPP PERITONEAL DIALYSATE FILTER |
| Classification | Peritoneal Dialysate Filter |
| Applicant | MILLIPORE CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KPP |
| CFR Regulation Number | 876.5630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-12-29 |
| Decision Date | 1981-03-13 |