510(k) Report

510(k) · Cleared

Cleared

E. Coli Pna Fish

K082068510(k) TraditionalCleared Jun 25, 2009338-day reviewClass I21 CFR 866.2660

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

Advandx, Inc. · JSS Kit, Identification, Enterobacteriaceae

Cleared on Jun 25, 2009 after a 338-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

Decided
Jun 25, 2009
Review
338 days
Class
Class I
Product code
JSS
Recalls
None
Predicates
0

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

FIG. 1 — Lineage of K082068Source: FDA 510(k) database · 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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What was it cleared against?

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

What descends from it?

No later submission names this one as a predicate yet.

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.

How does its category compare?

All JSS devices

JSS Kit, Identification, Enterobacteriaceae: FDA decisions, review times, recalls and adverse event reports over 20 years. 2009, this device’s year, is highlighted.

FDA decisions per year · JSS

1in 2015

2008: 12009: 42010: 12013: 12015: 1
2007high 4 (2009) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JSS

228in 2009

2009: 228 days median
2007high 228 (2009)2026

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

Recalls per year · JSS

1in 2022

2010: 22012: 32013: 12021: 12022: 1
2007high 3 (2012) · low 0 (2007)2026

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

Adverse event reports per year · JSS

1in 2023

2013: 12015: 12017: 32018: 32019: 32020: 82021: 92022: 22023: 1
2007high 9 (2021) · low 0 (2007)2025

MAUDE reports naming product code JSS, 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
20081—00
2009422800
20101—20
20110—00
20120—30
20131—11
20140—00
20151—01
20160—00
20170—03
20180—03
20190—03
20200—08
20210—19
20220—12
20230—01
20240—00
20250—00
20260—0—
Cite this page

510(k) Report. “K082068: E. Coli Pna Fish.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K082068

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Record history
  • FDA decision record loaded May 2, 2026
  • Page last updated Nov 3, 2026