510(k) Report

510(k) · Cleared

Cleared

Three Char. Test-Child & Worth 4 Dot Test Nearpt.

K874250510(k) TraditionalCleared Jan 11, 198884-day reviewClass I21 CFR 886.1880

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

Richmond Products, Inc. · HLP Target, Fusion And Stereoscopic

Cleared on Jan 11, 1988 after an 84-day review. FDA has not posted a summary or statement for it, so its predicates are not known.

Decided
Jan 11, 1988
Review
84 days
Class
Class I
Product code
HLP
Recalls
None
Predicates
0

FDA has not posted a summary or statement for it, so its predicates are not known.

FIG. 1 — Lineage of K874250Source: FDA 510(k) database · How lineage is built

Get the monthly Device Review Tracker

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

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

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

  • Candidate predicates for a device like this, rankedin the report
  • Recall history across each candidate’s familyin the report
Get a 510(k) Report

What was it cleared against?

FDA has not posted a summary or statement for it, so its predicates are not known.

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.

How does its category compare?

All HLP devices

HLP Target, Fusion And Stereoscopic: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · HLP

FDA has decided no HLP device since 2007.

Median 510(k) review, days · HLP

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

Recalls per year · HLP

No recall names HLP since 2007.

Adverse event reports per year · HLP

No MAUDE report names HLP since 2007.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20150—00
20160—00
20170—00
20180—00
20190—00
20200—00
20210—00
20220—00
20230—00
20240—00
20250—00
20260—0—

More from Richmond Products, Inc.

15 FDA decisions under this applicant name. See the company

  • K874252Kreda DiscRichmond Products, Inc. · 1988
  • K874251Worth 4 Dot Test Distance C/W Muscle LightRichmond Products, Inc. · 1988
  • K873907Confirmation TestsRichmond Products, Inc. · 1987
  • K873908H.R.R. Pseudoisochromatic Color Blindness Test BK.Richmond Products, Inc. · 1987
  • K873914Animated Fixation Toys (Distance and Nearpoint)Richmond Products, Inc. · 1987

Recent decisions in HLP

The HLP category page

  • K883471VKG 1000, Video KeratometerTechnitex, Inc. · 1988
  • K874251Worth 4 Dot Test Distance C/W Muscle LightRichmond Products, Inc. · 1988

https://510kreport.com/device/K874250 · printed Nov 4, 2026

Cite this page

510(k) Report. “K874250: Three Char. Test-Child & Worth 4 Dot Test Nearpt..” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K874250

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

Record history
  • FDA decision record loaded May 2, 2026
  • Page last updated Nov 3, 2026