# K960494: Euroline A312 Series of Behind the Ear Air Conduction Hearing Aids

- Pathway: 510(k) (Traditional)
- Applicant: Starkey Laboratories, Inc.
- Decided: Mar 1, 1996 after 31 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
Longest line of descent: 1 generation back to K940978 (1994). 1 ancestor in all.
1 later device descends from it; 1 cites 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)
- K940978: Starkey Euroline a Series, Starkey Laboratories, Inc. (1994) Summary page 1.

## Most influential descendants
- K963519: Euroline a-675 Seris (1996), 0 descendants of its own

## Indications for use
To assist in compensating for hearing loss by ampilifying sound as it comes near the ear.

Source page: https://510kreport.com/device/K960494
Methodology: https://510kreport.com/methodology