# K896750: Lofric (R), Lofric (R) Cath-Kit

- Pathway: 510(k) (Traditional)
- Applicant: Astra Meditec AB
- Decided: Aug 6, 1990 after 249 days
- Product code: KOD (Catheter, Urological)
- Device class: 2
- Regulation: 21 CFR 876.5130
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
69 later devices descend from it; 6 cite it directly.
0 of 70 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
- K012374: Modification to: Lofric Plus Single Use Urinary Catheter (2001), 54 descendants of its own
- K023254: Speedicath (2003), 53 descendants of its own
- K050874: Astra Tech AB Lofric Primo Single Use Urinary Catheter (2005), 33 descendants of its own
- K090960: Vapro Intermittent Catheter, Model 72062, 72082,72102, 72122, 72142, 72064, 72084, 72104, 72124,72144, 72164, 72184, (2009), 15 descendants of its own
- K110862: Vapro Plus Intermittent Catheter (2011), 14 descendants of its own

Source page: https://510kreport.com/device/K896750
Methodology: https://510kreport.com/methodology