# K091042: Crono S-Pid 50

- Pathway: 510(k) (Special)
- Applicant: Cane S.R.L.
- Decided: May 12, 2009 after 29 days
- Product code: FRN (Pump, Infusion)
- Device class: 2
- Regulation: 21 CFR 880.5725
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K982838 (1998). 5 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K052217: Crono Super Pid, Cane S.R.L. (2005) Summary page 1.
- K052218: Crono Five and Crono Pca 50, Cane S.R.L. (2005) Summary page 1.

## Most influential descendants
- K251105: Tetra (TM-20); Tetra (TM-50) (2025), 0 descendants of its own

## Indications for use
the Crono S-PID 50 has been designed for use in subcutaneous infusion of prescribed liquid medicines.

Source page: https://510kreport.com/device/K091042
Methodology: https://510kreport.com/methodology