# K192966: FlowMet

- Pathway: 510(k) (Special)
- Applicant: Laser Associated Sciences, Inc.
- Decided: Jan 10, 2020 after 79 days
- Product code: DPW (Flowmeter, Blood, Cardiovascular)
- Device class: 2
- Regulation: 21 CFR 870.2100
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 6 generations back to K905232 (1991). 7 ancestors in all.
No later device cites it as a predicate yet.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K182494: FlowMet-R, Laser Associated Sciences, Inc. (2019) Summary page 6.

## Indications for use
The FlowMet is a non-invasive probe that is affixed to the fingers or toes and intended to quantify tissue blood flow rate.

Source page: https://510kreport.com/device/K192966
Methodology: https://510kreport.com/methodology