KPP — Peritoneal Dialysate Filter Class II
FDA Device Classification
Classification Details
- Product Code
- KPP
- Device Class
- Class II
- Regulation Number
- 876.5630
- Submission Type
- Review Panel
- GU
- Medical Specialty
- Gastroenterology, Urology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K812615 | tri-med | TM-CAPD | January 5, 1982 |
| K803275 | millipore | KPP PERITONEAL DIALYSATE FILTER | March 13, 1981 |
| K800666 | liquid crystal products | QUIK-TEMP | May 8, 1980 |