510(k) Report

510(k) · Cleared

Cleared

Oculab Tonopen

K852774510(k) TraditionalCleared Aug 20, 198550-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

Oculab, Inc. · HKY Tonometer, Manual

Cleared on Aug 20, 1985 after a 50-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it.

Decided
Aug 20, 1985
Review
50 days
Class
Class II
Product code
HKY
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 2004: 1 descendant cleared1990200020102020
  1. This deviceK852774 Oculab TonopenOculab, Inc. · 1985
  2. Descendant · cites it directly · 0 of its ownK042099 Tonopach Ultrasonic Tonometer/Pachymeter Model P-201 (the Tonopach)Retinapharma Technologies, Inc. · 2004

Most influential descendants

Showing 1 of 1 · See all
  • K042099Tonopach Ultrasonic Tonometer/Pachymeter Model P-201 (the Tonopach)Retinapharma Technologies, Inc. · 2004 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K852774Oculab TonopenOculab, Inc.1985—
+1K042099Tonopach Ultrasonic Tonometer/Pachymeter Model P-201 (the Tonopach)Retinapharma Technologies, Inc.2004—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200410
FIG. 1 — Lineage of K852774, 1985–2004Source: 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), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in HKY? 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 HKY device

  1. #1 K241447 iCare ST500 (TA04)score 9.6 · 6 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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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? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K042099Tonopach Ultrasonic Tonometer/Pachymeter Model P-201 (the Tonopach)Retinapharma Technologies, Inc.20040

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?

  • Of its descendants, K042099 (Retinapharma Technologies, Inc., 2004) has gone furthest, with 0 descendants of its own.

How does its category compare?

All HKY devices

HKY Tonometer, Manual: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · HKY

3in 2024

2007: 22008: 12010: 12013: 12014: 32015: 22016: 32017: 22018: 32019: 12020: 22021: 12022: 22023: 12024: 3
2007high 3 (2014) · low 0 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HKY

128in 2024

2014: 123 days median2016: 226 days median2018: 77 days median2024: 128 days median
2007high 226 (2016) · low 77 (2018)2026

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

Recalls per year · HKY

2in 2014

2014: 2
2007high 2 (2014) · low 0 (2007)2026

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

Adverse event reports per year · HKY

1in 2019

2010: 22013: 12014: 32015: 12016: 22019: 1
2007high 3 (2014) · low 0 (2007)2025

MAUDE reports naming product code HKY, 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
20072—00
20081—00
20090—00
20101—02
20110—00
20120—00
20131—01
2014312323
20152—01
2016322602
20172—00
201837700
20191—01
20202—00
20211—00
20222—00
20231—00
2024312800
20250—00
20260—0—
Cite this page

510(k) Report. “K852774: Oculab Tonopen.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K852774

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