510(k) Report

510(k) · Cleared

Recalled · 2003

Abbott Imx Free T4

K902834510(k) TraditionalCleared Sep 7, 199071-day reviewClass II21 CFR 862.1695Recalls 1

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

Abbott Laboratories · CEC Radioimmunoassay, Free Thyroxine

Cleared on Sep 7, 1990 after a 71-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it. It has been recalled once.

Decided
Sep 7, 1990
Review
71 days
Class
Class II
Product code
CEC
Recalls
1
Predicates
0

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

Descendants, by year cleared 2003: 1 descendant cleared1990200020102020
  1. This deviceK902834 Abbott Imx Free T4Abbott Laboratories · 1990
  2. Descendant · cites it directly · 0 of its ownK030329 Fastpack Free T4 ImmunoassayQualigen, Inc. · 2003 · Recalled

Most influential descendants

Showing 1 of 1 · See all
  • K030329Fastpack Free T4 ImmunoassayQualigen, Inc. · 2003 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K902834Abbott Imx Free T4Abbott Laboratories1990—
+1K030329Fastpack Free T4 ImmunoassayQualigen, Inc.20031

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200310
FIG. 1 — Lineage of K902834, 1990–2003Source: 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 CEC? 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 CEC device

  1. #1 K240273 Access Free T4score 7.0 · 1 generation · no Class I recall
  2. #2 Held for the reportin the report
Get a 510(k) Report

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
K030329Fastpack Free T4 ImmunoassayQualigen, Inc.20030

Has anything in its family been recalled? (0 Class I)

Recalls of this device

DateClassRecallRoot causeReason
May 30, 2003Not classifiedZ-1131-03OtherThe Free T4 Controls, may yield control values that are high and outside of the package insert ranges.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • Of its descendants, K030329 (Qualigen, Inc., 2003) has gone furthest, with 0 descendants of its own.

How does its category compare?

All CEC devices

CEC Radioimmunoassay, Free Thyroxine: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · CEC

1in 2024

2007: 12008: 22009: 12012: 12013: 22014: 32015: 12016: 12017: 12018: 22023: 12024: 1
2007high 3 (2014) · low 0 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · CEC

238in 2014

2014: 238 days median
2007high 238 (2014)2026

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

Recalls per year · CEC

1in 2018

2010: 32013: 12018: 1
2007high 3 (2010) · low 0 (2007)2026

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

Adverse event reports per year · CEC

213in 2025

2009: 22010: 72011: 152012: 62013: 62014: 402015: 1662016: 1482017: 1962018: 1992019: 1672020: 1062021: 962022: 812023: 992024: 2762025: 213
2007high 276 (2024) · low 0 (2007)2025

MAUDE reports naming product code CEC, 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—00
20082—00
20091—02
20100—37
20110—015
20121—06
20132—16
20143238040
20151—0166
20161—0148
20171—0196
20182—1199
20190—0167
20200—0106
20210—096
20220—081
20231—099
20241—0276
20250—0213
20260—0—
Cite this page

510(k) Report. “K902834: Abbott Imx Free T4.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K902834

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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