# K842898: Curity I.V. Start Kit

- Pathway: 510(k) (Traditional)
- Applicant: The Kendal Co.
- Decided: Aug 17, 1984 after 25 days
- Product code: LRS (I.V. Start Kit)
- Device class: 2
- Regulation: 21 CFR 880.5200
- 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.
No later device cites it as a predicate yet.
0 of 1 device 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.

## Recalls of this device
- Apr 12, 2013 · Class III · Z-1303-2013: On March 26, 2013 Covidien received a recall notice from one of their suppliers CareFusion. CareFusion is recalling a variety of OTC drug products including the 10% Povidone Iodine SEPP Applicator whi

Source page: https://510kreport.com/device/K842898
Methodology: https://510kreport.com/methodology