# K063586: Moorflpi Full-Field Laser Perfusion Imager

- Pathway: 510(k) (Traditional)
- Applicant: Moor Instruments, Ltd.
- Decided: Jan 25, 2007 after 55 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: 3 generations back to K905232 (1991). 4 ancestors in all.
6 later devices descend from it; 2 cite it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K032841: Moorldi Infrared Laser Doppler Imager, Model MOORLD12-IR, Moor Instruments, Ltd. (2003) Summary page 1.

## Most influential descendants
- K120884: Pericam Psi (2012), 3 descendants of its own
- K182494: FlowMet-R (2019), 1 descendant of its own
- K122943: Moorflpi-2 Full-Field Laser Perfusion Imager (2013), 1 descendant of its own
- K233076: Laser Speckle Imaging System (RFLSI CZW) (2024), 0 descendants of its own
- K192966: FlowMet (2020), 0 descendants of its own

## Indications for use
The moorFLPI 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/K063586
Methodology: https://510kreport.com/methodology