Class Class II
NIKKICART (K221652)
Description
NIKKICART by Renal Care Dialysis Solutions, S.A. DE C.V., an FDA 510(k) cleared gastroenterology, urology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK221652
Clearance Date2023-03-03
Clearance TypeTraditional
Product CodeKPO
Regulation Number876.5820
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K221652
A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. NIKKICART (K221652) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K013724 | BICART | Gambro Renal Products | 2002 |
Trace the full predicate network for K221652
A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.