# K122943: Moorflpi-2 Full-Field Laser Perfusion Imager

- Pathway: 510(k) (Traditional)
- Applicant: Moor Instruments, Ltd.
- Decided: Jan 3, 2013 after 101 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.
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)
- K063586: Moorflpi Full-Field Laser Perfusion Imager, Moor Instruments, Ltd. (2007) Summary page 2.

## Most influential descendants
- K233076: Laser Speckle Imaging System (RFLSI CZW) (2024), 0 descendants of its own

## Indications for use
The moorFLPI-2 Full-Field Laser Perfusion Imager is intended for blood flow measurements in the microcirculation. This device is intended for clinical research use.

Source page: https://510kreport.com/device/K122943
Methodology: https://510kreport.com/methodology