# K853608: Neurometer

- Pathway: 510(k) (Traditional)
- Applicant: Neurotron, Inc.
- Decided: Jun 12, 1986 after 288 days
- Product code: LLN (Device, Vibration Threshold Measurement)
- Device class: 1
- Regulation: 21 CFR 882.1200
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
25 later devices descend from it; 4 cite it directly.
0 of 26 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K982359: NC-Stat (1998), 21 descendants of its own
- K013459: Modification of NC-Stat (2002), 20 descendants of its own
- K041320: Modification to NC-Stat (2004), 19 descendants of its own
- K060584: NC-Stat (2006), 18 descendants of its own
- K070109: Neurometrix Advance (2008), 15 descendants of its own

Source page: https://510kreport.com/device/K853608
Methodology: https://510kreport.com/methodology