# K181675: FORA MD6 Uric Acid Monitoring System, FORA MD6 Pro Uric Acid Monitoring System

- Pathway: 510(k) (Traditional)
- Applicant: Taidoc Technology Corporation
- Decided: Dec 10, 2018 after 168 days
- Product code: PTC (Uric Acid Test System For At Home Prescription Use)
- Device class: 1
- Regulation: 21 CFR 862.1775
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

Source page: https://510kreport.com/device/K181675
Methodology: https://510kreport.com/methodology