# K930328: Navigator & Traveler Evoked Postential Product

- Pathway: 510(k) (Traditional)
- Applicant: Bio-Logic Systems Corp.
- Decided: Jul 2, 1993 after 161 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
No predicates in its family tree.
23 later devices descend from it; 1 cites it directly.
0 of 24 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K992807: Bio-Logic Evoked Potential for Abaer I (1999), 22 descendants of its own
- K994149: Modification to Bio-Logic Evoked Potential for Abaer/ Navigator Pro. (1999), 21 descendants of its own
- K021895: Bio-Logic Master Evoked Response System (2002), 13 descendants of its own
- K070696: Interacoustics Assr, Eclipse System (Cabinet Name) (2007), 6 descendants of its own
- K021215: Bio-Logic Abaer Cub (2002), 5 descendants of its own

Source page: https://510kreport.com/device/K930328
Methodology: https://510kreport.com/methodology