# K073415: Nemus System; Nemus PC Peripheral

- Pathway: 510(k) (Traditional)
- Applicant: Eb Neuro S.P.A.
- Decided: May 23, 2008 after 171 days
- Product code: IKN (Electromyograph, Diagnostic)
- Device class: 2
- Regulation: 21 CFR 890.1375
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K922488 (1993). 2 ancestors in all.
40 later devices descend from it; 4 cite it directly.
0 of 43 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K922488: Phasis Electromyograph, Biosound, Inc. (1993) Summary page 1.
- K981405: Synergy LT, Oxford Instruments, Plc. (1998) Summary page 1.

## Most influential descendants
- K102610: Focus Emg Device (2011), 34 descendants of its own
- K112052: Carefusion Nicolet Edx (2012), 30 descendants of its own
- K162383: Cadwell Sierra Summit, Cadwell Sierra Ascent (2017), 12 descendants of its own
- K120979: Carefusion Nicolet Edx (2012), 12 descendants of its own
- K182542: The EPAD 2 System (2019), 9 descendants of its own

## Indications for use
NEMUS systems are diagnostic medical systems able to detect the electric signals produced by the peripheral nerve system and by skeletal muscles. The NEMUS system is intended to monitor, record and display the bioelectric signal produced by the muscles, to stimulate peripheral nerves, and to monitor, record and display the electrical activity produced by nerves to aid the clinician in the diagnosis and prognosis of neuromuscular diseases (EMG). The device may use electrical stimulus or sound stimulus for use in evoked response measurements (EP).

Source page: https://510kreport.com/device/K073415
Methodology: https://510kreport.com/methodology