510(k) Report

510(k) · Cleared

Cleared

Alko Tonometered Saline Control

K950902510(k) TraditionalCleared Mar 30, 199530-day reviewClass I21 CFR 862.1660

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

Alko Diagnostic Corp. · JJS Controls For Blood-Gases, (Assayed And Unassayed)

Cleared on Mar 30, 1995 after a 30-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
Mar 30, 1995
Review
30 days
Class
Class I
Product code
JJS
Recalls
None
Predicates
0

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

Descendants, by year cleared 2003: 1 descendant cleared1995200020052010201520202025
  1. This deviceK950902 Alko Tonometered Saline ControlAlko Diagnostic Corp. · 1995
  2. Descendant · cites it directly · 0 of its ownK033063 Mission ControlsDiamond Diagnostics, Inc. · 2003

Most influential descendants

Showing 1 of 1 · See all
  • K033063Mission ControlsDiamond Diagnostics, Inc. · 2003 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K950902Alko Tonometered Saline ControlAlko Diagnostic Corp.1995—
+1K033063Mission ControlsDiamond Diagnostics, Inc.2003—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200310
FIG. 1 — Lineage of K950902, 1995–2003Source: 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 JJS? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

  • Candidate predicates for a device like this, rankedin the report
  • 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
K033063Mission ControlsDiamond Diagnostics, Inc.20030

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, K033063 (Diamond Diagnostics, Inc., 2003) has gone furthest, with 0 descendants of its own.

How does its category compare?

All JJS devices

JJS Controls For Blood-Gases, (Assayed And Unassayed): FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · JJS

1in 2016

2013: 22015: 12016: 1
2007high 2 (2013) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JJS

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

Recalls per year · JJS

No recall names JJS since 2007.

Adverse event reports per year · JJS

1in 2018

2017: 12018: 1
2007high 1 (2017) · low 0 (2007)2025

MAUDE reports naming product code JJS, 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
20080—00
20090—00
20100—00
20110—00
20120—00
20132—00
20140—00
20151—00
20161—00
20170—01
20180—01
20190—00
20200—00
20210—00
20220—00
20230—00
20240—00
20250—00
20260—0—
Cite this page

510(k) Report. “K950902: Alko Tonometered Saline Control.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K950902

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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