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Bicarby Dialysate RFP-404 - Bicarby Dialysate RFP-456 (RFP-456-W)
FDA 510(k)Class II (US FDA 510(k))
510(k) K252180
Identifiers
- 510(k) Number
- K252180 FDA 510(k)
- FDA Product Code
- KPO FDA 510(k)
- Models / Variants
- Bicarby Dialysate RFP-404 (RFP-404-W) FDA 510(k)Bicarby Dialysate RFP-403 (RFP-403-W) FDA 510(k)Bicarby Dialysate RFP-403 (RFP-403-G) FDA 510(k)Bicarby Dialysate RFP-453 (RFP-453-W) FDA 510(k)Bicarby Dialysate RFP-453 (RFP-453-G) FDA 510(k)Bicarby Dialysate RFP-454 (RFP-454-W) FDA 510(k)Bicarby Dialysate RFP-454 (RFP-454-G) FDA 510(k)Bicarby Dialysate RFP-456 (RFP-456-W) FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 876.5820 FDA 510(k)
- Regulation Number
- 876.5820 FDA 510(k)
- Advisory Committee
- Gastroenterology, Urology FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Bicarby Dialysate RFP-404 - Bicarby Dialysate RFP-456 (RFP-456-W) by Fresenius Medical Care Renal Therapies Group, LLC — Class II — FDA_510K — listed in FDA…
Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K252180 | Class II | Active |
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Manufacturer
- Manufacturer
- Fresenius Medical Care Renal Therapies Group, LLC
Sources (1)
- FDA 510(k) K252180 24 fields · synced Jun 19, 2026