510(k) Report

510(k) · Cleared

Cleared

Reagent, Chloridometer Acid

K760394510(k) TraditionalCleared Nov 1, 197687-day reviewClass II21 CFR 862.1170

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

Bulcher Instruments · JFS Coulometric, Chloride

Cleared on Nov 1, 1976 after an 87-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it.

Decided
Nov 1, 1976
Review
87 days
Class
Class II
Product code
JFS
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 2013: 1 descendant cleared19801990200020102020
  1. This deviceK760394 Reagent, Chloridometer AcidBulcher Instruments · 1976
  2. Descendant · cites it directly · 0 of its ownK121823 Clinical Chloride Analyzer, Chloride Test System, Sweat Chloride…Wescor, Inc. · 2013

Most influential descendants

Showing 1 of 1 · See all
  • K121823Clinical Chloride Analyzer, Chloride Test System, Sweat Chloride Analyzer…Wescor, Inc. · 2013 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K760394Reagent, Chloridometer AcidBulcher Instruments1976—
+1K121823Clinical Chloride Analyzer, Chloride Test System, Sweat Chloride Analyzer…Wescor, Inc.2013—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201310
FIG. 1 — Lineage of K760394, 1976–2013Source: 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.

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  • Recall history across each candidate’s familyin 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? (1)

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

NumberDeviceApplicantDecidedDescendants
K121823Clinical Chloride Analyzer, Chloride Test System, Sweat Chloride Analyzer…Wescor, Inc.20130

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, K121823 (Wescor, Inc., 2013) has gone furthest, with 0 descendants of its own.

How does its category compare?

All JFS devices

JFS Coulometric, Chloride: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · JFS

1in 2013

2013: 1
2007high 1 (2013) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JFS

Too few JFS 510(k)s in any year since 2007 to give a median.

Recalls per year · JFS

No recall names JFS since 2007.

Adverse event reports per year · JFS

No MAUDE report names JFS since 2007.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—00
20090—00
20100—00
20110—00
20120—00
20131—00
20140—00
20150—00
20160—00
20170—00
20180—00
20190—00
20200—00
20210—00
20220—00
20230—00
20240—00
20250—00
20260—0—
Cite this page

510(k) Report. “K760394: Reagent, Chloridometer Acid.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K760394

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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