# K102433: Moorvms-Pres Pressure Cuff Controller

- Pathway: 510(k) (Traditional)
- Applicant: Moor Instruments, Ltd.
- Decided: Nov 18, 2010 after 84 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: 2 generations back to K951486 (1995). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K011899: PF 5050 Pressure Unit, Model PF 5050, Perimed AB (2001) Summary page 1.

## Indications for use
The moorVMS-PRES pressure cuff controller is a device for cuff inflation and deflation control and pressure measurement. It is intended to allow non-invasive measurement of skin perfusion pressure, pulse volume, systolic blood pressure and ankle/toe brachial pressure index when used with a laser Doppler monitor either manually by the operator or automatically by separate dedicated PC software.

Source page: https://510kreport.com/device/K102433
Methodology: https://510kreport.com/methodology