510(k) Report

510(k) · Cleared

Cleared

Eeg Mis Monitor Model # a-2000; Bis Engine

K011534510(k) SpecialCleared Jun 15, 200128-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

Aspect Medical Systems, Inc. · OLW Index-Generating Electroencephalograph Software

Cleared on Jun 15, 2001 after a 28-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 316 later devices descend from it.

Decided
Jun 15, 2001
Review
28 days
Class
Class II
Product code
OLW
Recalls
None
Predicates
0

316 later devices descend from it, 3 citing it directly.

Descendants, by year cleared 2003: 2 descendants cleared2002: 1 descendant cleared2004: 4 descendants cleared2005: 10 descendants cleared2006: 11 descendants cleared2008: 11 descendants cleared2007: 8 descendants cleared2013: 13 descendants cleared2015: 10 descendants cleared2011: 13 descendants cleared2016: 14 descendants cleared2012: 10 descendants cleared2009: 6 descendants cleared2010: 9 descendants cleared2017: 13 descendants cleared2018: 16 descendants cleared2023: 28 descendants cleared2014: 12 descendants cleared2024: 23 descendants cleared2021: 14 descendants cleared2026: 16 descendants cleared2019: 14 descendants cleared2022: 21 descendants cleared2020: 12 descendants cleared2025: 25 descendants cleared200020052010201520202025
  1. This deviceK011534 Eeg Mis Monitor Model # a-2000; Bis EngineAspect Medical Systems, Inc. · 2001
  2. Descendant · cites it directly · 304 of its ownK031694 Modification to Eeg Monitor with Bis, Model a-2000Aspect Medical Systems, Inc. · 2003
  3. Descendant · cites it directly · 303 of its ownK030267 Eeg Monitor with Bis, Model a-2000Aspect Medical Systems, Inc. · 2004
  4. Descendant · 2 generations on · 274 of its ownK040183 BISXAspect Medical Systems, Inc. · 2004
  5. Descendant · 3 generations on · 252 of its ownK041235 Philips MP20, MP30, MP40, MP50. MP60, MP70 and MP90 Intellivue…Philips Medizin Systeme Boeblingen GmbH · 2004
  6. Descendant · 4 generations on · 251 of its ownK042845 The Philips MP20, MP30, MP40, MP50, MP60, MP70, and MP90 Intellivue…Philips Medizin Systeme Boblingen GmbH · 2004

Showing 5 of 316 descendants. See all descendants

Descendants cleared per year

2002: 12003: 22004: 42005: 102006: 112007: 82008: 112009: 62010: 92011: 132012: 102013: 132014: 122015: 102016: 142017: 132018: 162019: 142020: 122021: 142022: 212023: 282024: 232025: 252026: 16
2002high 28 (2023) · low 1 (2002)2026

Most influential descendants

Showing 5 of 316 · See all
  • K031694Modification to Eeg Monitor with Bis, Model a-2000Aspect Medical Systems, Inc. · 2003 · cites it directly304descendants
  • K030267Eeg Monitor with Bis, Model a-2000Aspect Medical Systems, Inc. · 2004 · cites it directly303descendants
  • K040183BISXAspect Medical Systems, Inc. · 2004 · 2 generations on274descendants
  • K041235Philips MP20, MP30, MP40, MP50. MP60, MP70 and MP90 Intellivue Patient MonitorsPhilips Medizin Systeme Boeblingen GmbH · 2004 · 3 generations on252descendants
  • K042845The Philips MP20, MP30, MP40, MP50, MP60, MP70, and MP90 Intellivue Patient MonitorsPhilips Medizin Systeme Boblingen GmbH · 2004 · 4 generations on251descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K011534Eeg Mis Monitor Model # a-2000; Bis EngineAspect Medical Systems, Inc.2001—
+1K031694Modification to Eeg Monitor with Bis, Model a-2000Aspect Medical Systems, Inc.2003—
+1K030267Eeg Monitor with Bis, Model a-2000Aspect Medical Systems, Inc.2004—
+2K040183BISXAspect Medical Systems, Inc.2004—
+3K041235Philips MP20, MP30, MP40, MP50. MP60, MP70 and MP90 Intellivue Patient MonitorsPhilips Medizin Systeme Boeblingen GmbH2004—
+4K042845The Philips MP20, MP30, MP40, MP50, MP60, MP70, and MP90 Intellivue Patient…Philips Medizin Systeme Boblingen GmbH2004—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200210
200320
200440
2005100
2006110
200780
2008110
200960
201090
2011130
2012100
2013130
2014120
2015100
2016140
2017130
2018160
2019140
2020120
2021140
2022210
2023280
2024230
2025250
2026160
FIG. 1 — Lineage of K011534, 2001–2026Source: 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 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

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  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? (316)

See all 316

3 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K031694Modification to Eeg Monitor with Bis, Model a-2000Aspect Medical Systems, Inc.2003304
K030267Eeg Monitor with Bis, Model a-2000Aspect Medical Systems, Inc.2004303
K013389Datex-Ohmeda S/5 Bis Module, M-Bis and AccessoriesDatex-Ohmeda200210

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, K031694 (Aspect Medical Systems, Inc., 2003) has gone furthest, with 304 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—
Cite this page

510(k) Report. “K011534: Eeg Mis Monitor Model # a-2000; Bis Engine.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K011534

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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