# K021754: Apex Medical Digital Ems TS1311, TS1312

- Pathway: 510(k) (Special)
- Applicant: Apex Medical Corp.
- Decided: Jun 28, 2002 after 30 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’s file for it is a 510(k) statement, which names no predicate.

## 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

## Indications for use
Apex Medical Digital EMS is intended to be used in: 1. Relaxation of Muscle Spasm. 2. Prevention or retardation of disuse atrophy. 3. Increase local blood circulation. 4. Muscle re-education. 5. Immediate post surgical stimulation of calf muscles to prevent venous thrombosis. 6. Maintaining or increasing range of motion.

Source page: https://510kreport.com/device/K021754
Methodology: https://510kreport.com/methodology