# K923875: Sidekick 50 Plus and Sidekick 100 Plus

- Pathway: 510(k) (Traditional)
- Applicant: I-Flow Corp.
- Decided: May 13, 1993 after 283 days
- Product code: FRN (Pump, Infusion)
- Device class: 2
- Regulation: 21 CFR 880.5725
- 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.
15 later devices descend from it; 6 cite it directly.
1 of 16 devices in its family (counting itself) has 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
- K984146: Paragon Infusion (1999), 11 descendants of its own
- K984063: Paragon Basal/Bolus Administration Set (1999), 9 descendants of its own
- K020251: Paragon Infusion System (2002), 8 descendants of its own
- K052451: MPS Acacia Medflo Elastomeric Pump (2005), 5 descendants of its own
- K081905: Accuflow and Accuflux Elastomeric Infusion Pump (2008), 4 descendants of its own

## Recalls of this device
- Mar 5, 2003 · Not classified · Z-0709-03: Wrong component may result in over infusion of medications.

Source page: https://510kreport.com/device/K923875
Methodology: https://510kreport.com/methodology