510(k) Report

510(k) · Cleared

Recalled · Class II · 2019

Televix

K790692510(k) TraditionalCleared Apr 23, 197913-day reviewClass II21 CFR 892.1980Recalls 1

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

General Electrical Espanola, S.A. · KXJ Table, Radiologic

Cleared on Apr 23, 1979 after a 13-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 8 later devices descend from it. It has been recalled once.

Decided
Apr 23, 1979
Review
13 days
Class
Class II
Product code
KXJ
Recalls
1
Predicates
0

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

Descendants, by year cleared 2007: 1 descendant cleared2013: 1 descendant cleared2012: 1 descendant cleared2015: 2 descendants cleared2019: 1 descendant cleared2020: 1 descendant cleared2024: 1 descendant cleared19801990200020102020
  1. This deviceK790692 TelevixGeneral Electrical Espanola, S.A. · 1979
  2. Descendant · cites it directly · 7 of its ownK071546 EOSBiospace Med · 2007 · Recalled
  3. Descendant · 2 generations on · 6 of its ownK120721 EOSEos Imaging · 2012
  4. Descendant · 2 generations on · 5 of its ownK123740 EOSEos Imaging · 2013 · Recalled
  5. Descendant · 3 generations on · 4 of its ownK142773 EOS SystemEos Imaging · 2015
  6. Descendant · 4 generations on · 3 of its ownK152788 EOS SystemEos Imaging · 2015

Showing 5 of 8 descendants. See all descendants

Descendants cleared per year

2007: 12012: 12013: 12015: 22019: 12020: 12024: 1
2007high 2 (2015) · low 0 (2008)2026

Most influential descendants

Showing 5 of 8 · See all
  • K071546EOSBiospace Med · 2007 · cites it directly7descendants
  • K120721EOSEos Imaging · 2012 · 2 generations on6descendants
  • K123740EOSEos Imaging · 2013 · 2 generations on5descendants
  • K142773EOS SystemEos Imaging · 2015 · 3 generations on4descendants
  • K152788EOS SystemEos Imaging · 2015 · 4 generations on3descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K790692TelevixGeneral Electrical Espanola, S.A.1979—
+1K071546EOSBiospace Med20071
+2K120721EOSEos Imaging2012—
+2K123740EOSEos Imaging20131
+3K142773EOS SystemEos Imaging2015—
+4K152788EOS SystemEos Imaging2015—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200710
201210
201310
201520
201910
202010
202410
FIG. 1 — Lineage of K790692, 1979–2024Source: 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 KXJ? 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? (8)

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

NumberDeviceApplicantDecidedDescendants
K071546EOSBiospace Med20077

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

Recalls of this device

DateClassRecallRoot causeReason
Mar 29, 2019Class IIZ-1753-2019Device DesignThere has been a reported incident of a Distar CRT monitor that has fallen off the monitor wall mount related to product aging.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • Of its descendants, K071546 (Biospace Med, 2007) has gone furthest, with 7 descendants of its own.

How does its category compare?

All KXJ devices

KXJ Table, Radiologic: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · KXJ

FDA has decided no KXJ device since 2007.

Median 510(k) review, days · KXJ

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

Recalls per year · KXJ

4in 2019

2007: 12011: 12016: 42018: 12019: 42026 (partial year): 1
2007high 4 (2016) · low 0 (2008)2026

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

Adverse event reports per year · KXJ

9in 2025

2007: 142008: 402009: 62010: 52011: 192012: 52013: 52014: 12015: 22016: 12017: 122018: 312019: 42020: 22021: 92022: 502023: 122024: 82025: 9
2007high 50 (2022) · low 1 (2014)2025

MAUDE reports naming product code KXJ, 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—114
20080—040
20090—06
20100—05
20110—119
20120—05
20130—05
20140—01
20150—02
20160—41
20170—012
20180—131
20190—44
20200—02
20210—09
20220—050
20230—012
20240—08
20250—09
20260—1—

Recent decisions in KXJ

The KXJ category page

  • K050190ApolloVilla Sistemi Medicali S.P.A. · 200515 recalls
  • K963905Radiographic Itt TableX-Ray Technologies, Inc. · 1996
  • K955414XRT 400Wuestec Medical, Inc. · 1996
  • K951146Imaging TableSepta Corp. · 1995
  • K950068Carbon Fiber Couch InsertMedtec, Inc. · 1995

https://510kreport.com/device/K790692 · printed Nov 6, 2026

Cite this page

510(k) Report. “K790692: Televix.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K790692

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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