510(k) Report

510(k) · Cleared

Cleared

Laser Flare Cell Meter FC-1000

K880920510(k) TraditionalCleared Sep 27, 1988207-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

Kowa Optimed, Inc. · HJO Biomicroscope, Slit-Lamp, Ac-Powered

Cleared on Sep 27, 1988 after a 207-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 2 later devices descend from it.

Decided
Sep 27, 1988
Review
207 days
Class
Class II
Product code
HJO
Recalls
None
Predicates
0

2 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 2009: 1 descendant cleared2026: 1 descendant cleared1990200020102020
  1. This deviceK880920 Laser Flare Cell Meter FC-1000Kowa Optimed, Inc. · 1988
  2. Descendant · cites it directly · 1 of its ownK091039 Kowa, FM-600, Model LSS50Kowa Co., Ltd. · 2009
  3. Descendant · 2 generations on · 0 of its ownK261255 Kowa FM-600Kowa Company, Ltd. Chofu Factory · 2026

Most influential descendants

Showing 2 of 2 · See all
  • K091039Kowa, FM-600, Model LSS50Kowa Co., Ltd. · 2009 · cites it directly1descendant
  • K261255Kowa FM-600Kowa Company, Ltd. Chofu Factory · 2026 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K880920Laser Flare Cell Meter FC-1000Kowa Optimed, Inc.1988—
+1K091039Kowa, FM-600, Model LSS50Kowa Co., Ltd.2009—
+2K261255Kowa FM-600Kowa Company, Ltd. Chofu Factory2026—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200910
202610
FIG. 1 — Lineage of K880920, 1988–2026Source: 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 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? (2)

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

NumberDeviceApplicantDecidedDescendants
K091039Kowa, FM-600, Model LSS50Kowa Co., Ltd.20091

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, K091039 (Kowa Co., Ltd., 2009) has gone furthest, with 1 descendant of its own.

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. “K880920: Laser Flare Cell Meter FC-1000.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K880920

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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