# K003122: Smartflow, Model Sfip 2000

- Pathway: 510(k) (Traditional)
- Applicant: Florence Medical, Ltd.
- Decided: May 14, 2001 after 221 days
- Product code: DSK (Computer, Blood-Pressure)
- Device class: 2
- Regulation: 21 CFR 870.1110
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
49 later devices descend from it; 2 cite it directly.
0 of 50 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
- K012947: Smartflow (2001), 48 descendants of its own
- K020127: Smartflow Pulse Transmission Coefficient (2002), 47 descendants of its own
- K022188: Radianalyzer, Model 12710 (2002), 46 descendants of its own
- K042628: Modification to: Radianalyzer, Model 12711 (2005), 26 descendants of its own
- K031662: Pressure Wire Sensor, Models 12004/12304 (2003), 26 descendants of its own

Source page: https://510kreport.com/device/K003122
Methodology: https://510kreport.com/methodology