510(k) Report

510(k) · Cleared

Cleared

Sedline Sedation Monitor with Frontal Psi and Sedtrace Eeg Electrose Set

K051874510(k) SpecialCleared Sep 2, 200553-day reviewClass II21 CFR 882.1400

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

Physiometrix, Inc. · OLW Index-Generating Electroencephalograph Software

Cleared on Sep 2, 2005 as substantially equivalent to K033999 (Physiometrix, Inc., 2004) and 1 other predicate after a 53-day review. Its family tree reaches back 3 generations to 2000. 59 later devices descend from it.

Decided
Sep 2, 2005
Review
53 days
Class
Class II
Product code
OLW
Recalls
None
Predicates
2

Its longest line of descent runs back 3 generations to K001069 (2000). 4 ancestors in all. 59 later devices descend from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2002: 1 other ancestor2014: 2 descendants cleared2018: 2 descendants cleared2016: 2 descendants cleared2015: 1 descendant cleared2023: 6 descendants cleared2022: 9 descendants cleared2019: 5 descendants cleared2017: 2 descendants cleared2026: 6 descendants cleared2025: 8 descendants cleared2020: 5 descendants cleared2024: 10 descendants cleared2021: 1 descendant clearedK001069 · Model 4000 Eeg Monitor with Psi (PSA4000) · Physiometrix, Inc. · 2000K020671 · PSA4000 Eeg Monitor with Frontal Psi · Physiometrix, Inc. · 2002K033999 · Sedline with Frontal Psi · Physiometrix, Inc. · 2004200020052010201520202025
Other ancestors, by generationDescendants, by generation 1 generation back: 1 other ancestor 1 generation forward: 1 descendant2 generations forward: 2 descendants3 generations forward: 5 descendants4 generations forward: 6 descendants5 generations forward: 12 descendants6 generations forward: 21 descendants7 generations forward: 11 descendants8 generations forward: 1 descendant K033999 · Sedline with Frontal Psi · Physiometrix, Inc. · 2004K020671 · PSA4000 Eeg Monitor with Frontal Psi · Physiometrix, Inc. · 2002K001069 · Model 4000 Eeg Monitor with Psi (PSA4000) · Physiometrix, Inc. · 20000+5
  1. Root · 3 generations backK001069 Model 4000 Eeg Monitor with Psi (PSA4000)Physiometrix, Inc. · 2000
  2. 2 generations backK020671 PSA4000 Eeg Monitor with Frontal PsiPhysiometrix, Inc. · 2002
  3. 1 generation backK033999 Sedline with Frontal PsiPhysiometrix, Inc. · 2004
  4. This deviceK051874 Sedline Sedation Monitor with Frontal Psi and Sedtrace Eeg Electrose…Physiometrix, Inc. · 2005
  5. Descendant · cites it directly · 58 of its ownK140188 Masimo Root Monitoring SystemMasimo Corporation · 2014
  6. Descendant · 2 generations on · 51 of its ownK142394 Masimo Root Monitoring System and AccesoriesMasimo Corporation · 2014
  7. Descendant · 3 generations on · 24 of its ownK151644 Masimo Root Vital Signs Monitoring System and AccessoriesMasimo Corporation · 2016
  8. Descendant · 3 generations on · 24 of its ownK150314 Masimo MightySat Rx Fingertip Pulse OximeterMasimo Corporation · 2015
  9. Descendant · 4 generations on · 23 of its ownK181956 Masimo MightySat Rx Fingertip Pulse OximeterMasimo Corporation · 2019

Showing 5 of 59 descendants. See all descendants

Descendants cleared per year

2014: 22015: 12016: 22017: 22018: 22019: 52020: 52021: 12022: 92023: 62024: 102025: 82026: 6
2014high 10 (2024) · low 1 (2015)2026

Most influential descendants

Showing 5 of 59 · See all
  • K140188Masimo Root Monitoring SystemMasimo Corporation · 2014 · cites it directly58descendants
  • K142394Masimo Root Monitoring System and AccesoriesMasimo Corporation · 2014 · 2 generations on51descendants
  • K151644Masimo Root Vital Signs Monitoring System and AccessoriesMasimo Corporation · 2016 · 3 generations on24descendants
  • K150314Masimo MightySat Rx Fingertip Pulse OximeterMasimo Corporation · 2015 · 3 generations on24descendants
  • K181956Masimo MightySat Rx Fingertip Pulse OximeterMasimo Corporation · 2019 · 4 generations on23descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K001069Model 4000 Eeg Monitor with Psi (PSA4000)Physiometrix, Inc.2000—
−2K020671PSA4000 Eeg Monitor with Frontal PsiPhysiometrix, Inc.2002—
−1K033999Sedline with Frontal PsiPhysiometrix, Inc.2004—
0 (this device)K051874Sedline Sedation Monitor with Frontal Psi and Sedtrace Eeg Electrose SetPhysiometrix, Inc.2005—
+1K140188Masimo Root Monitoring SystemMasimo Corporation2014—
+2K142394Masimo Root Monitoring System and AccesoriesMasimo Corporation2014—
+3K151644Masimo Root Vital Signs Monitoring System and AccessoriesMasimo Corporation2016—
+3K150314Masimo MightySat Rx Fingertip Pulse OximeterMasimo Corporation2015—
+4K181956Masimo MightySat Rx Fingertip Pulse OximeterMasimo Corporation2019—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200210

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201420
201510
201620
201720
201820
201950
202050
202110
202290
202360
2024100
202580
202660
FIG. 1 — Lineage of K051874, 2000–2026Source: 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), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in OLW? 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 OLW device

  1. #1 K260880 SedLine Sedation Monitorscore 17.0 · 19 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (2)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K033999Sedline with Frontal Psi
Summary page 5
…le substrate. The SEDTrace connects to the patient cable with a custom connector. Predicate Device: SEDLine Sedation Monitor with Frontal PSI (K033999) PSArray 2 EEG Electrode Set (K020670) Similarities: The subject device is similar to the predicat…
Physiometrix, Inc.2004—
*K020670Model 4310 PSARRAY2 Eeg Electrode
Summary page 5
…the patient cable with a custom connector. Predicate Device: SEDLine Sedation Monitor with Frontal PSI (K033999) PSArray 2 EEG Electrode Set (K020670) Similarities: The subject device is similar to the predicate device in the following way(s): a.…
Physiometrix, Inc.2002—

What descends from it? (59)

See all 59

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

NumberDeviceApplicantDecidedDescendants
K140188Masimo Root Monitoring SystemMasimo Corporation201458

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?

  • The line of descent spans 5 years and passes through 1 company; a new generation was cleared every 1.6 years on median.
  • None of the 4 ancestors has a recall.
  • Of its descendants, K140188 (Masimo Corporation, 2014) has gone furthest, with 58 descendants of its own.

How does its category compare?

All OLW devices

OLW Index-Generating Electroencephalograph Software: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · OLW

1in 2024

2007: 32008: 22015: 12018: 12021: 12022: 12023: 12024: 12026 (partial year): 2
2007high 3 (2007) · low 0 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · OLW

105in 2007

2007: 105 days median
2007high 105 (2007)2026

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

Recalls per year · OLW

No recall names OLW since 2007.

Adverse event reports per year · OLW

73in 2025

2017: 32018: 32019: 62020: 152021: 152022: 272023: 182024: 932025: 73
2007high 93 (2024) · low 0 (2007)2025

MAUDE reports naming product code OLW, 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
2007310500
20082—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20151—00
20160—00
20170—03
20181—03
20190—06
20200—015
20211—015
20221—027
20231—018
20241—093
20250—073
20262—0—

What is it indicated for?

The SEDLine Sedation Monitor is indicated for use in the operating room (OR), intensive care unit (ICU), and clinical research laboratory. It is intended to monitor the state of the brain by real-time data acquisition and processing of EEG signals. The system includes the Patient State Index (PSI), a proprietary computed EEG variable that is related to the effect of anesthetic agents.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K051874: Sedline Sedation Monitor with Frontal Psi and Sedtrace Eeg Electrose Set.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K051874

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026