510(k) Report

510(k) · Cleared

Cleared

Avl Model 985 Electrolyte Analyzer

K870657510(k) TraditionalCleared May 12, 198783-day reviewClass II21 CFR 862.1600

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

Avl Scientific Corp. · CEM Electrode, Ion Specific, Potassium

Cleared on May 12, 1987 after an 83-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
May 12, 1987
Review
83 days
Class
Class II
Product code
CEM
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 deviceK870657 Avl Model 985 Electrolyte AnalyzerAvl Scientific Corp. · 1987
  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)K870657Avl Model 985 Electrolyte AnalyzerAvl Scientific Corp.1987—
+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 K870657, 1987–2026Source: 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 CEM? 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 CEM device

  1. #1 K253491 ISE indirect K for Gen.2; ISE indirect Na for…score 11.4 · 3 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 CEM devices

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

FDA decisions per year · CEM

1in 2025

2007: 12009: 12010: 32011: 32012: 42020: 12023: 22025: 12026 (partial year): 1
2007high 4 (2012) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · CEM

180in 2012

2010: 195 days median2011: 74 days median2012: 180 days median
2007high 195 (2010) · low 74 (2011)2026

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

Recalls per year · CEM

4in 2025

2008: 12010: 122011: 62016: 12019: 12020: 32021: 12023: 22025: 4
2007high 12 (2010) · low 0 (2007)2026

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

Adverse event reports per year · CEM

29in 2025

2007: 662008: 2452009: 792010: 1132011: 1262012: 452013: 372014: 42015: 72016: 62017: 322018: 132019: 252020: 272021: 182022: 162023: 302024: 422025: 29
2007high 245 (2008) · low 4 (2014)2025

MAUDE reports naming product code CEM, 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
20071—066
20080—1245
20091—079
2010319512113
20113746126
20124180045
20130—037
20140—04
20150—07
20160—16
20170—032
20180—013
20190—125
20201—327
20210—118
20220—016
20232—230
20240—042
20251—429
20261—0—
Cite this page

510(k) Report. “K870657: Avl Model 985 Electrolyte Analyzer.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K870657

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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