510(k) Report

510(k) · Cleared

Cleared

System 920 Argon/Dye Photocoagulator

K844357510(k) TraditionalCleared Jun 5, 1985208-day reviewClass II21 CFR 886.4390

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

Coherent Medical Group · HQF Laser, Ophthalmic

Cleared on Jun 5, 1985 after a 208-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 31 later devices descend from it.

Decided
Jun 5, 1985
Review
208 days
Class
Class II
Product code
HQF
Recalls
None
Predicates
0

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

Descendants, by year cleared 1997: 1 descendant cleared2008: 1 descendant cleared2005: 1 descendant cleared2009: 3 descendants cleared2010: 3 descendants cleared2011: 2 descendants cleared2013: 3 descendants cleared2015: 2 descendants cleared2019: 3 descendants cleared2012: 3 descendants cleared2017: 3 descendants cleared2016: 1 descendant cleared2023: 1 descendant cleared2022: 1 descendant cleared2025: 1 descendant cleared2024: 1 descendant cleared2018: 1 descendant cleared1990200020102020
  1. This deviceK844357 System 920 Argon/Dye PhotocoagulatorCoherent Medical Group · 1985
  2. Descendant · cites it directly · 30 of its ownK971950 Infinitech Multi-Spot Slit Lamp Laser AdapterInfinitech, Inc. · 1997
  3. Descendant · 2 generations on · 29 of its ownK043486 Pascal Photocoagulator, Product-Pascal-01Topcon Medical Laser Systems, Inc. · 2005
  4. Descendant · 3 generations on · 23 of its ownK091666 Pascal Photocoagulator, Pascal-USOptimedica Corporation · 2009
  5. Descendant · 4 generations on · 22 of its ownK092621 Pascal Streamline PhotocoagulatorTopcon Medical Laser Systems, Inc. · 2009
  6. Descendant · 2 generations on · 17 of its ownK081744 Pascal Synthesis Delivery SystemOptimedica Corporation · 2008

Showing 5 of 31 descendants. See all descendants

Descendants cleared per year

1997: 12005: 12008: 12009: 32010: 32011: 22012: 32013: 32015: 22016: 12017: 32018: 12019: 32022: 12023: 12024: 12025: 1
1997high 3 (2009) · low 0 (1998)2026

Most influential descendants

Showing 5 of 31 · See all
  • K971950Infinitech Multi-Spot Slit Lamp Laser AdapterInfinitech, Inc. · 1997 · cites it directly30descendants
  • K043486Pascal Photocoagulator, Product-Pascal-01Topcon Medical Laser Systems, Inc. · 2005 · 2 generations on29descendants
  • K091666Pascal Photocoagulator, Pascal-USOptimedica Corporation · 2009 · 3 generations on23descendants
  • K092621Pascal Streamline PhotocoagulatorTopcon Medical Laser Systems, Inc. · 2009 · 4 generations on22descendants
  • K081744Pascal Synthesis Delivery SystemOptimedica Corporation · 2008 · 2 generations on17descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K844357System 920 Argon/Dye PhotocoagulatorCoherent Medical Group1985—
+1K971950Infinitech Multi-Spot Slit Lamp Laser AdapterInfinitech, Inc.1997—
+2K043486Pascal Photocoagulator, Product-Pascal-01Topcon Medical Laser Systems, Inc.2005—
+3K091666Pascal Photocoagulator, Pascal-USOptimedica Corporation2009—
+4K092621Pascal Streamline PhotocoagulatorTopcon Medical Laser Systems, Inc.2009—
+2K081744Pascal Synthesis Delivery SystemOptimedica Corporation2008—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199710
200510
200810
200930
201030
201120
201230
201330
201520
201610
201730
201810
201930
202210
202310
202410
202510
FIG. 1 — Lineage of K844357, 1985–2025Source: 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 HQF? 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 HQF device

  1. #1 K251772 Navilas Laser System 577sl (156691)score 13.6 · 12 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? (31)

See all 31

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

NumberDeviceApplicantDecidedDescendants
K971950Infinitech Multi-Spot Slit Lamp Laser AdapterInfinitech, Inc.199730

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, K971950 (Infinitech, Inc., 1997) has gone furthest, with 30 descendants of its own.

How does its category compare?

All HQF devices

HQF Laser, Ophthalmic: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · HQF

3in 2025

2007: 42008: 32009: 72010: 22011: 42012: 52013: 62014: 32015: 42016: 32017: 32018: 12019: 42020: 42021: 12022: 72023: 52024: 32025: 32026 (partial year): 2
2007high 7 (2009) · low 1 (2018)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HQF

264in 2025

2007: 198 days median2008: 28 days median2009: 115 days median2011: 128 days median2012: 179 days median2013: 225 days median2014: 215 days median2015: 295 days median2016: 271 days median2017: 189 days median2019: 107 days median2020: 53 days median2022: 86 days median2023: 155 days median2024: 167 days median2025: 264 days median
2007high 295 (2015) · low 28 (2008)2026

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

Recalls per year · HQF

1in 2025

2007: 22008: 12009: 22010: 32011: 52012: 12013: 22014: 42025: 1
2007high 5 (2011) · low 0 (2015)2026

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

Adverse event reports per year · HQF

106in 2025

2007: 602008: 342009: 332010: 432011: 262012: 412013: 392014: 582015: 802016: 1082017: 772018: 822019: 662020: 722021: 1002022: 1112023: 922024: 752025: 106
2007high 111 (2022) · low 26 (2011)2025

MAUDE reports naming product code HQF, 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
20074198260
2008328134
20097115233
20102—343
20114128526
20125179141
20136225239
20143215458
20154295080
201632710108
20173189077
20181—082
20194107066
2020453072
20211—0100
20227860111
20235155092
20243167075
202532641106
20262—0—
Cite this page

510(k) Report. “K844357: System 920 Argon/Dye Photocoagulator.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K844357

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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