510(k) Report

510(k) · Cleared

Cleared

Insight Essentials DRF Digital Imaging System

K191310510(k) TraditionalCleared Jun 10, 201926-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

Imaging Engineering, LLC · JAA System, X-Ray, Fluoroscopic, Image-Intensified

Cleared on Jun 10, 2019 as substantially equivalent to K070390 (Virtual Imaging, Inc., 2007) after a 26-day review. Its family tree reaches back 3 generations to 1991. 2 later devices descend from it.

Decided
Jun 10, 2019
Review
26 days
Class
Class II
Product code
JAA
Recalls
None
Predicates
1

Its longest line of descent runs back 3 generations to K911454 (1991). 4 ancestors in all. 2 later devices descend from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 1996: 1 other ancestor2020: 1 descendant cleared2025: 1 descendant clearedK911454 · FC2000 · S & S Inficon, Inc. · 1991K012490 · Orion Digital Imaging System · Infimed, Inc. · 2002K070390 · Fluoropro RF Digital Imaging System · Virtual Imaging, Inc. · 20071990200020102020
Other ancestors, by generationDescendants, by generation 3 generations back: 1 other ancestor 1 generation forward: 1 descendant2 generations forward: 1 descendant K070390 · Fluoropro RF Digital Imaging System · Virtual Imaging, Inc. · 2007K012490 · Orion Digital Imaging System · Infimed, Inc. · 2002K911454 · FC2000 · S & S Inficon, Inc. · 19910
  1. Root · 3 generations backK911454 FC2000S & S Inficon, Inc. · 1991
  2. 2 generations backK012490 Orion Digital Imaging SystemInfimed, Inc. · 2002
  3. 1 generation backK070390 Fluoropro RF Digital Imaging SystemVirtual Imaging, Inc. · 2007
  4. This deviceK191310 Insight Essentials DRF Digital Imaging SystemImaging Engineering, LLC · 2019
  5. Descendant · cites it directly · 1 of its ownK200396 Insight Enhanced DRF Digital Imaging SystemImaging Engineering, LLC · 2020
  6. Descendant · 2 generations on · 0 of its ownK251650 Insight Enhanced™ DRF (EN-1002-01)Imaging Engineering, LLC · 2025

Most influential descendants

Showing 2 of 2 · See all
  • K200396Insight Enhanced DRF Digital Imaging SystemImaging Engineering, LLC · 2020 · cites it directly1descendant
  • K251650Insight Enhanced™ DRF (EN-1002-01)Imaging Engineering, LLC · 2025 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K911454FC2000S & S Inficon, Inc.1991—
−2K012490Orion Digital Imaging SystemInfimed, Inc.2002—
−1K070390Fluoropro RF Digital Imaging SystemVirtual Imaging, Inc.2007—
0 (this device)K191310Insight Essentials DRF Digital Imaging SystemImaging Engineering, LLC2019—
+1K200396Insight Enhanced DRF Digital Imaging SystemImaging Engineering, LLC2020—
+2K251650Insight Enhanced™ DRF (EN-1002-01)Imaging Engineering, LLC2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199610

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202010
202510
FIG. 1 — Lineage of K191310, 1991–2025Source: 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
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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
*K070390Fluoropro RF Digital Imaging System
Summary page 4
…JAA and LLZ Predicate Device Trade Name: FluoroPRO RF Digital Imaging System 510(k) Clearance #: K070390 Clearance date: 02/02/2007 Classification Name: Image Intensified Fluoroscopic X-ray S…
Virtual Imaging, Inc.2007—

What descends from it? (2)

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

NumberDeviceApplicantDecidedDescendants
K200396Insight Enhanced DRF Digital Imaging SystemImaging Engineering, LLC20201

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 28 years and passes through 4 companies; a new generation was cleared every 10.6 years on median.
  • None of the 4 ancestors has a recall.
  • Of its descendants, K200396 (Imaging Engineering, LLC, 2020) has gone furthest, with 1 descendant of its own.

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. 2019, 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?

Intended for use by a qualified/trained doctor or technician on both adult and pediatric subjects for obtaining fluoroscopic radiographic images of the skull, spinal column, chest, abdomen, extremities, and other body parts.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K191310: Insight Essentials DRF Digital Imaging System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K191310

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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