510(k) Report

510(k) · Cleared

Cleared

Nexus DRF Digital X-Ray Imaging System (with Paxscan 4343CB)

K130318510(k) SpecialCleared Apr 22, 201373-day reviewClass II21 CFR 892.1650

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

Varian Medical Systems, X-Ray Products-Infimed · JAA System, X-Ray, Fluoroscopic, Image-Intensified

Cleared on Apr 22, 2013 as substantially equivalent to K103416 (Infimed, Inc., 2011) after a 73-day review. Its family tree reaches back 6 generations to 1981. 15 later devices descend from it.

Decided
Apr 22, 2013
Review
73 days
Class
Class II
Product code
JAA
Recalls
None
Predicates
1

Its longest line of descent runs back 6 generations to K803130 (1981). 18 ancestors in all. 15 later devices descend from it, 4 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2002: 1 other ancestor1998: 3 other ancestors1996: 1 other ancestor1991: 1 other ancestor1997: 1 other ancestor1994: 2 other ancestors1992: 1 other ancestor1986: 1 other ancestor1988: 1 other ancestor2019: 4 descendants cleared2016: 1 descendant cleared2017: 3 descendants cleared2026: 3 descendants cleared2018: 1 descendant cleared2022: 1 descendant cleared2023: 1 descendant cleared2025: 1 descendant clearedK803130 · Multix U. Bucky Table X-Ray Unit · Siemens Corp. · 1981 · recalledK971452 · Multix Top/Pro Radiographic X-Ray Table · Siemens Medical Solutions USA, Inc. · 1997 · recalledK983732 · Thorax FD and Multix FD · Siemens Medical Solutions USA, Inc. · 1999 · recalledK992794 · Stingray DR, Model 1 · Infimed, Inc. · 1999K093066 · I5 Digital X-Ray Imaging System, Model I5 · Infimed, Inc. · 2010K103416 · Nexus DRF Digital X-Ray Imaging System · Infimed, Inc. · 201119801990200020102020
Other ancestors, by generationDescendants, by generation 3 generations back: 1 other ancestor4 generations back: 5 other ancestors5 generations back: 5 other ancestors6 generations back: 1 other ancestor 1 generation forward: 4 descendants2 generations forward: 3 descendants3 generations forward: 3 descendants4 generations forward: 2 descendants5 generations forward: 2 descendants6 generations forward: 1 descendant K103416 · Nexus DRF Digital X-Ray Imaging System · Infimed, Inc. · 2011K093066 · I5 Digital X-Ray Imaging System, Model I5 · Infimed, Inc. · 2010K992794 · Stingray DR, Model 1 · Infimed, Inc. · 1999K983732 · Thorax FD and Multix FD · Siemens Medical Solutions USA, Inc. · 1999 · recalledK971452 · Multix Top/Pro Radiographic X-Ray Table · Siemens Medical Solutions USA, Inc. · 1997 · recalledK803130 · Multix U. Bucky Table X-Ray Unit · Siemens Corp. · 1981 · recalled−50+5
  1. Root · 6 generations backK803130 Multix U. Bucky Table X-Ray UnitSiemens Corp. · 1981 · Recalled
  2. 5 generations backK971452 Multix Top/Pro Radiographic X-Ray TableSiemens Medical Solutions USA, Inc. · 1997 · Recalled
  3. 4 generations backK983732 Thorax FD and Multix FDSiemens Medical Solutions USA, Inc. · 1999 · Recalled
  4. 3 generations backK992794 Stingray DR, Model 1Infimed, Inc. · 1999
  5. 2 generations backK093066 I5 Digital X-Ray Imaging System, Model I5Infimed, Inc. · 2010
  6. 1 generation backK103416 Nexus DRF Digital X-Ray Imaging SystemInfimed, Inc. · 2011
  7. This deviceK130318 Nexus DRF Digital X-Ray Imaging System (with Paxscan 4343CB)Varian Medical Systems, X-Ray Products-Infimed · 2013
  8. Descendant · cites it directly · 6 of its ownK162529 DigiX FDXAllengers Medical Systems Limited · 2017
  9. Descendant · 2 generations on · 5 of its ownK192541 DigiX FDXAllengers Medical Systems Limited · 2019
  10. Descendant · cites it directly · 5 of its ownK161459 Nexus DRTM Digital X-ray Imaging System (with PaxScan 4336Wv4)Varian Medical Systems, X-Ray Products-Infimed · 2016
  11. Descendant · 3 generations on · 4 of its ownK223060 DigiX FDXAllengers Medical Systems Limited · 2022
  12. Descendant · 2 generations on · 4 of its ownK171138 Nexus DR Digital X-ray Imaging SystemVarex Imaging Corporation · 2017

Showing 5 of 15 descendants. See all descendants

Descendants cleared per year

2016: 12017: 32018: 12019: 42022: 12023: 12025: 12026: 3
2016high 4 (2019) · low 0 (2020)2026

Most influential descendants

Showing 5 of 15 · See all
  • K162529DigiX FDXAllengers Medical Systems Limited · 2017 · cites it directly6descendants
  • K192541DigiX FDXAllengers Medical Systems Limited · 2019 · 2 generations on5descendants
  • K161459Nexus DRTM Digital X-ray Imaging System (with PaxScan 4336Wv4)Varian Medical Systems, X-Ray Products-Infimed · 2016 · cites it directly5descendants
  • K223060DigiX FDXAllengers Medical Systems Limited · 2022 · 3 generations on4descendants
  • K171138Nexus DR Digital X-ray Imaging SystemVarex Imaging Corporation · 2017 · 2 generations on4descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K803130Multix U. Bucky Table X-Ray UnitSiemens Corp.19811
−5K971452Multix Top/Pro Radiographic X-Ray TableSiemens Medical Solutions USA, Inc.19978
−4K983732Thorax FD and Multix FDSiemens Medical Solutions USA, Inc.19991
−3K992794Stingray DR, Model 1Infimed, Inc.1999—
−2K093066I5 Digital X-Ray Imaging System, Model I5Infimed, Inc.2010—
−1K103416Nexus DRF Digital X-Ray Imaging SystemInfimed, Inc.2011—
0 (this device)K130318Nexus DRF Digital X-Ray Imaging System (with Paxscan 4343CB)Varian Medical Systems, X-Ray Products-Infimed2013—
+1K162529DigiX FDXAllengers Medical Systems Limited2017—
+2K192541DigiX FDXAllengers Medical Systems Limited2019—
+1K161459Nexus DRTM Digital X-ray Imaging System (with PaxScan 4336Wv4)Varian Medical Systems, X-Ray Products-Infimed2016—
+3K223060DigiX FDXAllengers Medical Systems Limited2022—
+2K171138Nexus DR Digital X-ray Imaging SystemVarex Imaging Corporation2017—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198610
198810
199110
199210
199420
199610
199710
199830
200210

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201610
201730
201810
201940
202210
202310
202510
202630
FIG. 1 — Lineage of K130318, 1981–2026Source: 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), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in JAA? 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 JAA device

  1. #1 K253103 Nexus DRF Digital X-ray Imaging Systemscore 13.2 · 7 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (1)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K103416Nexus DRF Digital X-Ray Imaging System
Summary page 1
…ing System (with PaxScan 4343C8)JAA, MQB Predicate Device: 510(k) Number: Product Codes: Nexus DRF Digital X-ray Imaging System K103416 JAA, MQB Device Description: The InfiMed j5Tm Digital X-ray Imaging System is a high resolution dig…
Infimed, Inc.2011—

Also cleared against K103416: 1 other device →

What descends from it? (15)

See all 15

4 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K162529DigiX FDXAllengers Medical Systems Limited20176
K161459Nexus DRTM Digital X-ray Imaging System (with PaxScan 4336Wv4)Varian Medical Systems, X-Ray Products-Infimed20165
K253103Nexus DRF Digital X-ray Imaging SystemVarex Imaging Corporation20260
K191504PowerDRRadiology Information Systems, Inc.20190

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?

  • The line of descent spans 32 years and passes through 4 companies; a new generation was cleared every 2.1 years on median.
  • 8 of the 18 ancestors have a recall of any class.
  • Of its descendants, K162529 (Allengers Medical Systems Limited, 2017) has gone furthest, with 6 descendants of its own.
  • 1 other device also cites its predicate K103416.

How does its category compare?

All JAA devices

JAA System, X-Ray, Fluoroscopic, Image-Intensified: FDA decisions, review times, recalls and adverse event reports over 20 years. 2013, this device’s year, is highlighted.

FDA decisions per year · JAA

2in 2025

2007: 12008: 62010: 12011: 42012: 12013: 62014: 62015: 32016: 22017: 12018: 32019: 62020: 42021: 62022: 12023: 22024: 32025: 22026 (partial year): 1
2007high 6 (2008) · low 0 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JAA

89in 2024

2008: 18 days median2011: 48 days median2013: 129 days median2014: 276 days median2015: 197 days median2018: 30 days median2019: 49 days median2020: 39 days median2021: 104 days median2024: 89 days median
2007high 276 (2014) · low 18 (2008)2026

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

Recalls per year · JAA

4in 2025

2007: 352008: 212009: 182010: 62011: 72012: 22013: 32014: 12015: 12016: 72017: 32018: 12019: 22020: 22021: 22022: 52023: 92024: 22025: 4
2007high 35 (2007) · low 1 (2014)2026

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

Adverse event reports per year · JAA

33in 2025

2007: 9,5172008: 9,4842009: 12,0402010: 5,8032011: 14,0002012: 11,6842013: 13,7062014: 10,2652015: 2,9222016: 352017: 562018: 362019: 492020: 392021: 352022: 342023: 412024: 252025: 33
2007high 14,000 (2011) · low 25 (2024)2025

MAUDE reports naming product code JAA, 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—359,517
2008618219,484
20090—1812,040
20101—65,803
2011448714,000
20121—211,684
20136129313,706
20146276110,265
2015319712,922
20162—735
20171—356
2018330136
2019649249
2020439239
20216104235
20221—534
20232—941
2024389225
20252—433
20261—0—

What is it indicated for?

The InfiMed iSTM Digital X-ray Imaging System is a high resolution digital imaging system intended to replace conventional film techniques, or existing digital systems, in multipurpose or dedicated applications specified below. The i5TM Digital X-ray Imaging System enables an operator to acquire, display, process, export images to portable media, send images over a network for long term storage and distribute hardcopy images with a laser printer. Image…

Read the full statement (183 words)

The InfiMed iSTM Digital X-ray Imaging System is a high resolution digital imaging system intended to replace conventional film techniques, or existing digital systems, in multipurpose or dedicated applications specified below. The i5TM Digital X-ray Imaging System enables an operator to acquire, display, process, export images to portable media, send images over a network for long term storage and distribute hardcopy images with a laser printer. Image processing algorithms enable the operator to bring out diagnostic details difficult to see using conventional imaging techniques. Images can be stored locally for temporary storage. The iS5TM Digital X-ray Imaging System has the ability to interface with a variety of image receptors from CCD cameras to commercially available flat panel detectors. The major system components include an image receptor, computer, monitor and imaging software.

For the DR application, the InfiMed i5TM Digital X-ray Imaging System is intended for use in general radiographic examinations and applications (excluding fluoroscopy, angiography, and mammography).

For the RF/DSA application, the InfiMed iSTM Digital X-ray Imaging System is intended for use where general fluoroscopy, interventional fluoroscopy or angiography imaging procedures are performed.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K130318: Nexus DRF Digital X-Ray Imaging System (with Paxscan 4343CB).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K130318

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026