510(k) Report

510(k) · Cleared

Cleared

Avl Model 984 Electrolyte Analyzer

K862819510(k) TraditionalCleared Aug 29, 198636-day reviewClass II21 CFR 862.1665

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

Avl Scientific Corp. · JGS Electrode, Ion Specific, Sodium

Cleared on Aug 29, 1986 after a 36-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 48 later devices descend from it.

Decided
Aug 29, 1986
Review
36 days
Class
Class II
Product code
JGS
Recalls
None
Predicates
0

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

Descendants, by year cleared 1996: 1 descendant cleared2008: 3 descendants cleared1997: 1 descendant cleared2009: 1 descendant cleared2012: 5 descendants cleared2003: 1 descendant cleared2018: 1 descendant cleared2011: 3 descendants cleared2020: 2 descendants cleared2005: 5 descendants cleared1998: 3 descendants cleared2000: 1 descendant cleared1999: 1 descendant cleared2015: 3 descendants cleared2006: 1 descendant cleared2004: 1 descendant cleared2013: 4 descendants cleared2010: 1 descendant cleared2021: 2 descendants cleared2014: 1 descendant cleared2017: 1 descendant cleared2025: 1 descendant cleared2016: 2 descendants cleared2024: 1 descendant cleared2026: 1 descendant cleared2023: 1 descendant cleared1990200020102020
  1. This deviceK862819 Avl Model 984 Electrolyte AnalyzerAvl Scientific Corp. · 1986
  2. Descendant · cites it directly · 47 of its ownK961458 Avl 9180 Electrolyte AnalyzerAvl Scientific Corp. · 1996 · Recalled
  3. Descendant · 2 generations on · 38 of its ownK972673 Avl 9181 Electrolyte AnalyzerAvl Scientific Corp. · 1997 · Recalled
  4. Descendant · 3 generations on · 31 of its ownK992859 ABL700 Series Analyzer with Autocheck ModuleRadiometer America, Inc. · 2000 · Recalled
  5. Descendant · 4 generations on · 29 of its ownK041874 ABL800 FlexRadiometer Medical Aps · 2004 · Recalled
  6. Descendant · 5 generations on · 18 of its ownK050869 Modification to ABL800 FlexRadiometer Medical Aps · 2005 · Recalled

Showing 5 of 48 descendants. See all descendants

Descendants cleared per year

1996: 11997: 11998: 31999: 12000: 12003: 12004: 12005: 52006: 12008: 32009: 12010: 12011: 32012: 52013: 42014: 12015: 32016: 22017: 12018: 12020: 22021: 22023: 12024: 12025: 12026: 1
1996high 5 (2005) · low 0 (2001)2026

Most influential descendants

Showing 5 of 48 · See all
  • K961458Avl 9180 Electrolyte AnalyzerAvl Scientific Corp. · 1996 · cites it directly47descendants
  • K972673Avl 9181 Electrolyte AnalyzerAvl Scientific Corp. · 1997 · 2 generations on38descendants
  • K992859ABL700 Series Analyzer with Autocheck ModuleRadiometer America, Inc. · 2000 · 3 generations on31descendants
  • K041874ABL800 FlexRadiometer Medical Aps · 2004 · 4 generations on29descendants
  • K050869Modification to ABL800 FlexRadiometer Medical Aps · 2005 · 5 generations on18descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K862819Avl Model 984 Electrolyte AnalyzerAvl Scientific Corp.1986—
+1K961458Avl 9180 Electrolyte AnalyzerAvl Scientific Corp.19961
+2K972673Avl 9181 Electrolyte AnalyzerAvl Scientific Corp.19977
+3K992859ABL700 Series Analyzer with Autocheck ModuleRadiometer America, Inc.20004
+4K041874ABL800 FlexRadiometer Medical Aps200422
+5K050869Modification to ABL800 FlexRadiometer Medical Aps20051

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199610
199710
199830
199910
200010
200310
200410
200550
200610
200830
200910
201010
201130
201250
201340
201410
201530
201620
201710
201810
202020
202120
202310
202410
202510
202610
FIG. 1 — Lineage of K862819, 1986–2026Source: 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 JGS? 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 JGS device

  1. #1 K252475 ABL90 FLEX PLUS Systemscore 12.2 · 4 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? (48)

See all 48

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

NumberDeviceApplicantDecidedDescendants
K961458Avl 9180 Electrolyte AnalyzerAvl Scientific Corp.199647

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, K961458 (Avl Scientific Corp., 1996) has gone furthest, with 47 descendants of its own.

How does its category compare?

All JGS devices

JGS Electrode, Ion Specific, Sodium: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · JGS

3in 2023

2008: 22009: 22010: 12011: 32012: 12013: 22014: 12015: 12016: 42017: 12018: 32019: 32020: 22022: 12023: 32026 (partial year): 1
2007high 4 (2016) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JGS

347in 2023

2011: 191 days median2016: 198 days median2018: 180 days median2019: 58 days median2023: 347 days median
2007high 347 (2023) · low 58 (2019)2026

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

Recalls per year · JGS

4in 2023

2007: 72008: 12010: 12011: 12012: 22013: 52015: 12019: 52020: 12021: 12023: 4
2007high 7 (2007) · low 0 (2009)2026

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

Adverse event reports per year · JGS

64in 2025

2007: 332008: 32009: 572010: 3612011: 9122012: 4122013: 5102014: 2512015: 1582016: 842017: 2922018: 1582019: 1052020: 892021: 912022: 602023: 982024: 962025: 64
2007high 912 (2011) · low 3 (2008)2025

MAUDE reports naming product code JGS, 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—733
20082—13
20092—057
20101—1361
201131911912
20121—2412
20132—5510
20141—0251
20151—1158
20164198084
20171—0292
201831800158
20193585105
20202—189
20210—191
20221—060
20233347498
20240—096
20250—064
20261—0—
Cite this page

510(k) Report. “K862819: Avl Model 984 Electrolyte Analyzer.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K862819

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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