# K832714: Verimed Myoexorciser

- Pathway: 510(k) (Traditional)
- Applicant: Verimed Holdings, Inc.
- Decided: Oct 28, 1983 after 77 days
- Product code: HCC (Device, Biofeedback)
- Device class: 2
- Regulation: 21 CFR 882.5050
- 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
- K943535: Model ME 300 Muscle Tester (1997), 0 descendants of its own
- K963202: Mega ME 3000 Professional Muscle Tester (1997), 0 descendants of its own

Source page: https://510kreport.com/device/K832714
Methodology: https://510kreport.com/methodology