# K950319: Resound (R) Personal Hearing System ED-3 Encore

- Pathway: 510(k) (Traditional)
- Applicant: Resound Corp.
- Decided: Feb 8, 1995 after 13 days
- Product code: ESD (Hearing Aid, Air-Conduction, Prescription)
- Device class: 1
- Regulation: 21 CFR 874.3300
- 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
- K960680: Resound Personal Hearing Systems Edr Encore Series Models Edr-E, Edr-ES, Edr-EV, & Edr-P1 (1996), 0 descendants of its own
- K960684: Hearing Aid - Air Conduction (1996), 0 descendants of its own

Source page: https://510kreport.com/device/K950319
Methodology: https://510kreport.com/methodology