510(k) Report

510(k) · Cleared

Cleared

Euroline a-675 Seris

K963519510(k) TraditionalCleared Sep 27, 199624-day reviewClass I21 CFR 874.3300

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Starkey Laboratories, Inc. · ESD Hearing Aid, Air-Conduction, Prescription

Cleared on Sep 27, 1996 as substantially equivalent to K960494 (Starkey Laboratories, Inc., 1996) after a 24-day review. Its family tree reaches back 2 generations to 1994.

Decided
Sep 27, 1996
Review
24 days
Class
Class I
Product code
ESD
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K940978 (1994). No later device cites it as a predicate yet.

  1. Root · 2 generations backK940978 Starkey Euroline a SeriesStarkey Laboratories, Inc. · 1994
  2. 1 generation backK960494 Euroline A312 Series of Behind the Ear Air Conduction Hearing AidsStarkey Laboratories, Inc. · 1996
  3. This deviceK963519 Euroline a-675 SerisStarkey Laboratories, Inc. · 1996
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K940978Starkey Euroline a SeriesStarkey Laboratories, Inc.1994—
−1K960494Euroline A312 Series of Behind the Ear Air Conduction Hearing AidsStarkey Laboratories, Inc.1996—
0 (this device)K963519Euroline a-675 SerisStarkey Laboratories, Inc.1996—
FIG. 1 — Lineage of K963519, 1994–1996Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in ESD? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new ESD device

  1. #1 K232999 Lyric4 Hearing Aidscore 8.4 · 5 generations · no Class I recall
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What was it cleared against? (2)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K960494Euroline A312 Series of Behind the Ear Air Conduction Hearing Aids
Summary page 1
…WER: 8/26/96 P27 e K9635/7 Ae675 TSP, Ae675 Sequel Air Conduction Behind-the-Ear hearing aids -Substantially equivalent to the Starkey A-312 Series BTE Hearing Aids (K960494) To assist in compensating for hearing loss by amplifying sound as it comes near the ear . Adjustable volume control, Microphon…
Starkey Laboratories, Inc.1996—
*—Starkey Laboratories Euroline A-13 Series BTE Hearing aids
Named without a submission number
—

What descends from it?

No later submission names this one as a predicate yet.

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 2 years and passes through 1 company; a new generation was cleared every 1.8 years on median.
  • None of the 2 ancestors has a recall.

How does its category compare?

All ESD devices

ESD Hearing Aid, Air-Conduction, Prescription: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · ESD

1in 2024

2008: 12013: 12024: 1
2007high 1 (2008) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · ESD

Too few ESD 510(k)s in any year since 2007 to give a median.

Recalls per year · ESD

2in 2019

2010: 12018: 12019: 2
2007high 2 (2019) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · ESD

53in 2025

2007: 132008: 132009: 32010: 12011: 32012: 62013: 372014: 42015: 62016: 72017: 42018: 122019: 92020: 52021: 42022: 42023: 82024: 162025: 53
2007high 53 (2025) · low 1 (2010)2025

MAUDE reports naming product code ESD, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—013
20081—013
20090—03
20100—11
20110—03
20120—06
20131—037
20140—04
20150—06
20160—07
20170—04
20180—112
20190—29
20200—05
20210—04
20220—04
20230—08
20241—016
20250—053
20260—0—

What is it indicated for?

To assist in compensating for hearing loss by amplifying sound as it comes near the ear.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K963519: Euroline a-675 Seris.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K963519

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026