# K002339: Aems V, Ems-1000, Model TS-140500 and Aems VI, Ems-1000 Plus, Model TS-140600

- Pathway: 510(k) (Traditional)
- Applicant: Apex Medical Corp.
- Decided: Aug 24, 2001 after 388 days
- Product code: IPF (Stimulator, Muscle, Powered)
- Device class: 2
- Regulation: 21 CFR 890.5850
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 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
- K071320: Everlife Powered Muscle Stimulator, Model E-100204, E-100504, E-100509, E-100804, E-201111, E-201211, E-201311 (2007), 0 descendants of its own

Source page: https://510kreport.com/device/K002339
Methodology: https://510kreport.com/methodology