510(k) Report

510(k) · Cleared

Cleared

Bio-Logic Sleepscan Netlink

K003681510(k) SpecialCleared Dec 21, 200021-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

Bio-Logic Systems Corp. · OLV Standard Polysomnograph With Electroencephalograph

Cleared on Dec 21, 2000 after a 21-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 of the 479 devices in its family, counting itself, has a Class I recall. 478 later devices descend from it.

Decided
Dec 21, 2000
Review
21 days
Class
Class II
Product code
OLV
Recalls
None
Predicates
0

478 later devices descend from it, 2 citing it directly. 1 of the 479 devices in this family, counting this one, has a Class I recall.

Descendants, by year cleared 2005: 3 descendants cleared2002: 1 descendant cleared2004: 1 descendant cleared2017: 18 descendants cleared2010: 1 descendant cleared2008: 1 descendant cleared2011: 3 descendants cleared2006: 2 descendants cleared2014: 5 descendants cleared2018: 23 descendants cleared2012: 3 descendants cleared2019: 31 descendants cleared2013: 5 descendants cleared2016: 9 descendants cleared2020: 24 descendants cleared2015: 9 descendants cleared2021: 42 descendants cleared, 1 with a Class I recall12022: 49 descendants cleared2023: 65 descendants cleared2025: 64 descendants cleared2026: 57 descendants cleared2024: 62 descendants cleared200020052010201520202025
  1. This deviceK003681 Bio-Logic Sleepscan NetlinkBio-Logic Systems Corp. · 2000
  2. Descendant · cites it directly · 471 of its ownK021807 Grass-Telefactor AS40 Amplifier SystemGrass Instrument Co. · 2002
  3. Descendant · 2 generations on · 460 of its ownK050798 Eclipse Neurological WorkstationAxon Systems, Inc. · 2005
  4. Descendant · 3 generations on · 450 of its ownK061113 OrthomonAxon Systems, Inc. · 2006
  5. Descendant · 3 generations on · 426 of its ownK061639 Eclipse TCD Neurovascular Workstation; Elclipse Neurological…Axon Systems, Inc. · 2006
  6. Descendant · 4 generations on · 418 of its ownK111520 Ipc Powerease SystemMedtronic Xomed, Inc. · 2011 · Recalled

Showing 5 of 478 descendants. See all descendants

Descendants cleared per year

2002: 12004: 12005: 32006: 22008: 12010: 12011: 32012: 32013: 52014: 52015: 92016: 92017: 182018: 232019: 312020: 242021: 422022: 492023: 652024: 622025: 642026: 57
2002high 65 (2023) · low 0 (2003)2026

Class I recalls in this family

Most influential descendants

Showing 5 of 478 · See all
  • K021807Grass-Telefactor AS40 Amplifier SystemGrass Instrument Co. · 2002 · cites it directly471descendants
  • K050798Eclipse Neurological WorkstationAxon Systems, Inc. · 2005 · 2 generations on460descendants
  • K061113OrthomonAxon Systems, Inc. · 2006 · 3 generations on450descendants
  • K061639Eclipse TCD Neurovascular Workstation; Elclipse Neurological Workstation with TCD and…Axon Systems, Inc. · 2006 · 3 generations on426descendants
  • K111520Ipc Powerease SystemMedtronic Xomed, Inc. · 2011 · 4 generations on418descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K003681Bio-Logic Sleepscan NetlinkBio-Logic Systems Corp.2000—
+1K021807Grass-Telefactor AS40 Amplifier SystemGrass Instrument Co.2002—
+2K050798Eclipse Neurological WorkstationAxon Systems, Inc.2005—
+3K061113OrthomonAxon Systems, Inc.2006—
+3K061639Eclipse TCD Neurovascular Workstation; Elclipse Neurological Workstation with…Axon Systems, Inc.2006—
+4K111520Ipc Powerease SystemMedtronic Xomed, Inc.20112

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200210
200410
200530
200620
200810
201010
201130
201230
201350
201450
201590
201690
2017180
2018230
2019310
2020240
2021421
2022490
2023650
2024620
2025640
2026570
FIG. 1 — Lineage of K003681, 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), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

1 device in this family has a Class I recall. 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 OLV device

  1. #1 K241288 Noxturnal Webscore 17.3 · 10 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? (478)

See all 478

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

NumberDeviceApplicantDecidedDescendants
K021807Grass-Telefactor AS40 Amplifier SystemGrass Instrument Co.2002471
K052066Ceegraph/Sleepscan Netlink TravelerBio-Logic Systems Corp.20055

Has anything in its family been recalled? (1 Class I)

No FDA recall names this device.

Relatives with a Class I recall

Class I is FDA’s most serious recall class. A recall in the family tree is context for this device, not evidence about it.

  • K211616ExcelsiusHubGlobus Medical, Inc. · 2021 · 9 generations on · ◆ in the 2021 descendants bar of FIG. 11 Class I recall

What does this lineage say?

  • Of its descendants, K021807 (Grass Instrument Co., 2002) has gone furthest, with 471 descendants of its own.

How does its category compare?

All OLV devices

OLV Standard Polysomnograph With Electroencephalograph: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · OLV

1in 2025

2008: 22010: 12011: 22013: 12015: 12017: 32018: 32020: 22022: 12024: 22025: 12026 (partial year): 2
2007high 3 (2017) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · OLV

141in 2018

2017: 83 days median2018: 141 days median
2007high 141 (2018) · low 83 (2017)2026

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

Recalls per year · OLV

No recall names OLV since 2007.

Adverse event reports per year · OLV

1in 2025

2013: 12016: 42018: 32019: 12021: 32022: 32023: 22024: 22025: 1
2007high 4 (2016) · low 0 (2007)2025

MAUDE reports naming product code OLV, 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
20070—00
20082—00
20090—00
20101—00
20112—00
20120—00
20131—01
20140—00
20151—00
20160—04
201738300
2018314103
20190—01
20202—00
20210—03
20221—03
20230—02
20242—02
20251—01
20262—0—
Cite this page

510(k) Report. “K003681: Bio-Logic Sleepscan Netlink.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K003681

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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