# K102194: Solcart B

- Pathway: 510(k) (Traditional)
- Applicant: B. Braun Avitum AG
- Decided: Apr 25, 2011 after 264 days
- Product code: KPO (Dialysate Concentrate For Hemodialysis (Liquid Or Powder))
- Device class: 2
- Regulation: 21 CFR 876.5820
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K873155 (1987). 4 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K072760: Solcart B, B. Braun Medizintechnologie GmbH (2008) Summary page 1.

## Most influential descendants
- K202508: Hemo-Lyte C Cartridge (2022), 0 descendants of its own

## Indications for use
Solcart B Powder Dialysis Concentrate is intended for use in bicarbonate hemodialysis for acute and chronic renal failure, or acute intoxication with dialyzable substances.

Source page: https://510kreport.com/device/K102194
Methodology: https://510kreport.com/methodology