510(k) Report

510(k) · Cleared

Cleared

Non-Contact Tonometer, Model NT-4000

K031733510(k) TraditionalCleared Dec 4, 2003183-day reviewClass II21 CFR 886.1930

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

Nidek, Inc. · HKX Tonometer, Ac-Powered

Cleared on Dec 4, 2003 as substantially equivalent to K913189 (Nidek, Inc., 1991) after a 183-day review. Its family tree reaches back 1 generation to 1991.

Decided
Dec 4, 2003
Review
183 days
Class
Class II
Product code
HKX
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K913189 (1991). No later device cites it as a predicate yet.

K913189 · Nidek Model NT-1000 · Nidek, Inc. · 19911990199520002005
K913189 · Nidek Model NT-1000 · Nidek, Inc. · 19910
  1. Root · 1 generation backK913189 Nidek Model NT-1000Nidek, Inc. · 1991
  2. This deviceK031733 Non-Contact Tonometer, Model NT-4000Nidek, Inc. · 2003
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K913189Nidek Model NT-1000Nidek, Inc.1991—
0 (this device)K031733Non-Contact Tonometer, Model NT-4000Nidek, Inc.2003—
FIG. 1 — Lineage of K031733, 1991–2003Source: 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 HKX? 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 HKX device

  1. #1 K253039 Auto Kerato-Refracto Tonometer TRK-3 Omniascore 11.5 · 5 generations · no Class I recall
  2. #2 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (1)

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
*K913189Nidek Model NT-1000
Summary page 1
…predicate device: Predicate Device Manufacturer 510(k) No. Date Cleared Model NT-1000 Non- Nidek Co. Ltd. K913189 October 15, Contact Tonometer 1991…
Nidek, Inc.1991—

Also cleared against K913189: 1 other device →

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?

  • Its one ancestor has no recall.
  • 1 other device also cites its predicate K913189.

How does its category compare?

All HKX devices

HKX Tonometer, Ac-Powered: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · HKX

1in 2025

2008: 22009: 12010: 12011: 12012: 12015: 12017: 12018: 12019: 32023: 12025: 1
2007high 3 (2019) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HKX

290in 2019

2019: 290 days median
2007high 290 (2019)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · HKX

No recall names HKX since 2007.

Adverse event reports per year · HKX

1in 2015

2008: 12010: 12015: 1
2007high 1 (2008) · low 0 (2007)2025

MAUDE reports naming product code HKX, 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—00
20082—01
20091—00
20101—01
20111—00
20121—00
20130—00
20140—00
20151—01
20160—00
20171—00
20181—00
2019329000
20200—00
20210—00
20220—00
20231—00
20240—00
20251—00
20260—0—

What is it indicated for?

The Nidek Model NT-4000 is a non-contact tonometer that is indicated for use in the measurement of intraocular pressure of the human eye.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K031733: Non-Contact Tonometer, Model NT-4000.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K031733

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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