510(k) Report

510(k) · Cleared

Cleared

UL UHD-Clear View 4K Camera System (UL-3Chip 4K)

K250462510(k) TraditionalCleared Aug 11, 2025174-day reviewClass II21 CFR 876.1500

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

Univlabs Technologies Private Limited · FET Endoscopic Video Imaging System/Component, Gastroenterology-Urology

Cleared on Aug 11, 2025 as substantially equivalent to K201135 (KARL STORZ Endoscopy-America, Inc., 2020) after a 174-day review. Its family tree reaches back 5 generations to 1995.

Decided
Aug 11, 2025
Review
174 days
Class
Class II
Product code
FET
Recalls
None
Predicates
1

Its longest line of descent runs back 5 generations to K944620 (1995). 6 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 5 generations backK944620 Series 400 Gastroenterology SystemMarks & Murase · 1995 · Recalled
  2. 4 generations backK102466 Fujinon Epx-4440HD Digital Video ProcessorFujinon, Inc. · 2011
  3. 3 generations backK131953 IMAGE1 SpiesKARL STORZ Endoscopy-America, Inc. · 2013 · Recalled
  4. 2 generations backK160044 Image1 SPIES SystemKarl Storz Endoscopy America, Inc. · 2016
  5. 1 generation backK201135 Image1 S CCU, Image1 S 4U Camera HeadKARL STORZ Endoscopy-America, Inc. · 2020
  6. This deviceK250462 UL UHD-Clear View 4K Camera System (UL-3Chip 4K)Univlabs Technologies Private Limited · 2025
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K944620Series 400 Gastroenterology SystemMarks & Murase19952
−4K102466Fujinon Epx-4440HD Digital Video ProcessorFujinon, Inc.2011—
−3K131953IMAGE1 SpiesKARL STORZ Endoscopy-America, Inc.20131
−2K160044Image1 SPIES SystemKarl Storz Endoscopy America, Inc.2016—
−1K201135Image1 S CCU, Image1 S 4U Camera HeadKARL STORZ Endoscopy-America, Inc.2020—
0 (this device)K250462UL UHD-Clear View 4K Camera System (UL-3Chip 4K)Univlabs Technologies Private Limited2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200710
FIG. 1 — Lineage of K250462, 1995–2025Source: 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 FET? 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 FET device

  1. #1 K242067 Visera Elite Iii Video System Center Olympus…score 18.4 · 12 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
*K201135Image1 S CCU, Image1 S 4U Camera Head
Summary page 5
…r 876.1500 Product Code(s) FET I Legally Marketed Predicate Devices 21 CFR 807.92(a)(3) Predicate # Predicate Trade Name (Primary Predicate is listed first) Product Code K201135 Image1 S CCU (TC200US, TC201US, TC300US, TC301US, FET TC302US, TC304US); Image1 S 4U Camera Head (TH120) Device Description Summa…
KARL STORZ Endoscopy-America, Inc.2020—

Also cleared against K201135: 1 other device →

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.

What does this lineage say?

  • The line of descent spans 30 years and passes through 5 companies; a new generation was cleared every 4.6 years on median.
  • 2 of the 6 ancestors have a recall of any class.
  • 1 other device also cites its predicate K201135.

How does its category compare?

All FET devices

FET Endoscopic Video Imaging System/Component, Gastroenterology-Urology: FDA decisions, review times, recalls and adverse event reports over 20 years. 2025, this device’s year, is highlighted.

FDA decisions per year · FET

6in 2025

2007: 12008: 22009: 22010: 12011: 22012: 22013: 22015: 22016: 12017: 32018: 32019: 32020: 52021: 12022: 22023: 12024: 22025: 62026 (partial year): 3
2007high 6 (2025) · low 0 (2014)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FET

166in 2025

2017: 119 days median2018: 98 days median2019: 25 days median2020: 106 days median2025: 166 days median2026 (partial year): 69 days median
2007high 166 (2025) · low 25 (2019)2026

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

Recalls per year · FET

1in 2024

2023: 22024: 1
2007high 2 (2023) · low 0 (2007)2026

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

Adverse event reports per year · FET

14,530in 2025

2007: 22008: 12009: 62010: 32011: 72012: 112013: 82014: 32015: 32016: 252017: 662018: 672019: 722020: 3,0432021: 5,3002022: 6,1562023: 8,1992024: 13,1532025: 14,530
2007high 14,530 (2025) · low 1 (2008)2025

MAUDE reports naming product code FET, 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—02
20082—01
20092—06
20101—03
20112—07
20122—011
20132—08
20140—03
20152—03
20161—025
20173119066
2018398067
2019325072
2020510603,043
20211—05,300
20222—06,156
20231—28,199
20242—113,153
20256166014,530
20263690—

What is it indicated for?

The UL UHD-Clear View 4K Camera System (UL-3Chip 4K), consisting of a Camera Control Unit and an Endoscopic Camera Head, is indicated for use with compatible endoscopes to provide visualization during general endoscopic procedures. These procedures may involve the visual inspection of internal anatomical structures to support diagnostic or therapeutic interventions. Patient suitability for particular endoscopic procedures must be determined by the responsible physician based on the individual’s clinical condition.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K250462: UL UHD-Clear View 4K Camera System (UL-3Chip 4K).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K250462

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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