# K883239: Capd Ultraviolet (U.V.) Germicidal Exchange Dev Sys

- Pathway: 510(k) (Traditional)
- Applicant: Baxter Healthcare Corp
- Decided: Oct 21, 1988 after 81 days
- Product code: KDJ (Set, Administration, For Peritoneal Dialysis, Disposable)
- Device class: 2
- Regulation: 21 CFR 876.5630
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 2 cite it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K151620: Firefly Peritoneal Dialysis Connector Disinfection System (2016), 0 descendants of its own
- K961825: Ultraset/3L Capd Disposable Disconnect Y-Set Models 5C4366 & 5C4493 (1996), 0 descendants of its own

## Recalls of this device
- Nov 5, 2004 · Not classified · Z-0301-05: Disconnection of the tubing at the clamp level of the UV Flash Transfer Set.

Source page: https://510kreport.com/device/K883239
Methodology: https://510kreport.com/methodology