# K843486: Vibrameter

- Pathway: 510(k) (Traditional)
- Applicant: Somedic AB
- Decided: Dec 24, 1984 after 109 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.
2 later devices descend from it; 2 cite it directly.
0 of 3 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
- K141208: Dynamic Neuroscreening Device (2014), 0 descendants of its own
- K030829: VPT Meter (2003), 0 descendants of its own

Source page: https://510kreport.com/device/K843486
Methodology: https://510kreport.com/methodology