# K120884: Pericam Psi

- Pathway: 510(k) (Traditional)
- Applicant: Perimed AB
- Decided: Jul 3, 2012 after 102 days
- Product code: DPT (Probe, Blood-Flow, Extravascular)
- Device class: 2
- Regulation: 21 CFR 870.2120
- 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 K905232 (1991). 5 ancestors in all.
3 later devices descend from it; 2 cite it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K920844: Pim 1.0 Laser Doppler Perfusion Imager, Lisca Development AB (1992) Summary page 3.
- K063586: Moorflpi Full-Field Laser Perfusion Imager, Moor Instruments, Ltd. (2007) Summary page 5.

## Most influential descendants
- K182494: FlowMet-R (2019), 1 descendant of its own
- K192966: FlowMet (2020), 0 descendants of its own
- K181269: iCertainty (2018), 0 descendants of its own

## Indications for use
The PeriCam PSI is intended for non-invasive two-dimensional imaging of peripheral tissue blood perfusion.

Source page: https://510kreport.com/device/K120884
Methodology: https://510kreport.com/methodology