510(k) Report

510(k) · Cleared

Cleared

904 Slit Lamp

K953965510(k) TraditionalCleared Sep 27, 199536-day reviewClass II21 CFR 886.1850

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

Clement Clarke, Inc. · HJO Biomicroscope, Slit-Lamp, Ac-Powered

Cleared on Sep 27, 1995 after a 36-day review. FDA has not posted a summary or statement for it, so its predicates are not known.

Decided
Sep 27, 1995
Review
36 days
Class
Class II
Product code
HJO
Recalls
None
Predicates
0

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

FIG. 1 — Lineage of K953965Source: FDA 510(k) database · 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 HJO? 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 HJO device

  1. #1 K253834 Visuref 600score 13.1 · 8 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?

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 HJO devices

HJO Biomicroscope, Slit-Lamp, Ac-Powered: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · HJO

1in 2024

2007: 12008: 42009: 32010: 52011: 22013: 22014: 102015: 22016: 52017: 92018: 22020: 12022: 12024: 12026 (partial year): 2
2007high 10 (2014) · low 0 (2012)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HJO

232in 2017

2008: 117 days median2009: 91 days median2010: 121 days median2014: 196 days median2016: 243 days median2017: 232 days median
2007high 243 (2016) · low 91 (2009)2026

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

Recalls per year · HJO

1in 2018

2013: 22015: 22018: 1
2007high 2 (2013) · low 0 (2007)2026

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

Adverse event reports per year · HJO

20in 2025

2007: 12008: 32009: 32010: 22011: 52012: 72013: 162014: 42015: 82016: 152017: 152018: 112019: 132020: 192021: 142022: 62023: 182024: 182025: 20
2007high 20 (2025) · low 1 (2007)2025

MAUDE reports naming product code HJO, 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
20071—01
2008411703
200939103
2010512102
20112—05
20120—07
20132—216
20141019604
20152—28
20165243015
20179232015
20182—111
20190—013
20201—019
20210—014
20221—06
20230—018
20241—018
20250—020
20262—0—
Cite this page

510(k) Report. “K953965: 904 Slit Lamp.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K953965

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