510(k) Report

510(k) · Cleared

Cleared

ISE/NA+

K912648510(k) TraditionalCleared Jul 17, 199130-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

Boehringer Mannheim Corp. · JGS Electrode, Ion Specific, Sodium

Cleared on Jul 17, 1991 after a 30-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 21 later devices descend from it.

Decided
Jul 17, 1991
Review
30 days
Class
Class II
Product code
JGS
Recalls
None
Predicates
0

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

Descendants, by year cleared 1996: 1 descendant cleared2006: 3 descendants cleared2013: 2 descendants cleared2005: 1 descendant cleared2008: 1 descendant cleared2010: 1 descendant cleared2012: 1 descendant cleared2011: 5 descendants cleared2007: 2 descendants cleared2014: 1 descendant cleared2021: 1 descendant cleared2019: 1 descendant cleared2015: 1 descendant cleared1990200020102020
  1. This deviceK912648 ISE/NA+Boehringer Mannheim Corp. · 1991
  2. Descendant · cites it directly · 20 of its ownK963627 (Modified Version) Integra Ion Selective Electrode (Ise) ModuleRoche Diagnostic Systems, Inc. · 1996
  3. Descendant · 2 generations on · 15 of its ownK052007 Abx Pentra 400 Clinical Chemistry Analyzer (Option: I.S.E. Module)Horiba Abx · 2005 · Recalled
  4. Descendant · 3 generations on · 3 of its ownK060854 Abx Pentra 400: LipoproteinsHoriba Abx · 2006 · Recalled
  5. Descendant · 3 generations on · 2 of its ownK123171 Abx Pentra Calcium as CP, Abx Pentra Urine Control L/H, Abx Pentra…Horiba Abx Sas · 2013
  6. Descendant · 2 generations on · 1 of its ownK123726 Cobas 8000 Ise Indirect NA, K, CI for Gen. 2Roche Diagnostics · 2013

Showing 5 of 21 descendants. See all descendants

Descendants cleared per year

1996: 12005: 12006: 32007: 22008: 12010: 12011: 52012: 12013: 22014: 12015: 12019: 12021: 1
1996high 5 (2011) · low 0 (1997)2026

Most influential descendants

Showing 5 of 21 · See all
  • K963627(Modified Version) Integra Ion Selective Electrode (Ise) ModuleRoche Diagnostic Systems, Inc. · 1996 · cites it directly20descendants
  • K052007Abx Pentra 400 Clinical Chemistry Analyzer (Option: I.S.E. Module)Horiba Abx · 2005 · 2 generations on15descendants
  • K060854Abx Pentra 400: LipoproteinsHoriba Abx · 2006 · 3 generations on3descendants
  • K123171Abx Pentra Calcium as CP, Abx Pentra Urine Control L/H, Abx Pentra Multical, Abx Pentra…Horiba Abx Sas · 2013 · 3 generations on2descendants
  • K123726Cobas 8000 Ise Indirect NA, K, CI for Gen. 2Roche Diagnostics · 2013 · 2 generations on1descendant
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K912648ISE/NA+Boehringer Mannheim Corp.1991—
+1K963627(Modified Version) Integra Ion Selective Electrode (Ise) ModuleRoche Diagnostic Systems, Inc.1996—
+2K052007Abx Pentra 400 Clinical Chemistry Analyzer (Option: I.S.E. Module)Horiba Abx20056
+3K060854Abx Pentra 400: LipoproteinsHoriba Abx20062
+3K123171Abx Pentra Calcium as CP, Abx Pentra Urine Control L/H, Abx Pentra Multical…Horiba Abx Sas2013—
+2K123726Cobas 8000 Ise Indirect NA, K, CI for Gen. 2Roche Diagnostics2013—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199610
200510
200630
200720
200810
201010
201150
201210
201320
201410
201510
201910
202110
FIG. 1 — Lineage of K912648, 1991–2021Source: 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? (21)

See all 21

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

NumberDeviceApplicantDecidedDescendants
K963627(Modified Version) Integra Ion Selective Electrode (Ise) ModuleRoche Diagnostic Systems, Inc.199620

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, K963627 (Roche Diagnostic Systems, Inc., 1996) has gone furthest, with 20 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. “K912648: ISE/NA+.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K912648

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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