510(k) Report

510(k) · Cleared

Cleared

Smith & Nephew Images Arthroscope/Ent Endoscope

K970247510(k) TraditionalCleared Mar 21, 199758-day reviewClass II21 CFR 874.4760

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

Smith & Nephew, Inc. · EOB Nasopharyngoscope (Flexible Or Rigid)

Cleared on Mar 21, 1997 after a 58-day review. The FDA summary names its predicate without a number.

Decided
Mar 21, 1997
Review
58 days
Class
Class II
Product code
EOB
Recalls
None
Predicates
0

The FDA summary names its predicate without a number.

FIG. 1 — Lineage of K970247Source: FDA 510(k) database · 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 EOB? 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 EOB device

  1. #1 K253184 Video Rhinolaryngoscope System (Disposable…score 14.4 · 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? (6)

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
*—Sinuscopes
Named without a submission number
—
*—Video components
Named without a submission number
—
*—Surgical cameras
Named without a submission number
—
*—Illuminators
Named without a submission number
—
*—Accessories
Named without a submission number
—
*—ENT surgical hand instruments
Named without a submission number
—

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.

How does its category compare?

All EOB devices

EOB Nasopharyngoscope (Flexible Or Rigid): FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · EOB

3in 2025

2007: 42008: 42009: 12010: 12011: 42012: 12014: 32015: 32016: 32017: 62018: 62019: 82020: 32021: 22022: 62023: 32024: 22025: 32026 (partial year): 5
2007high 8 (2019) · low 0 (2013)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · EOB

192in 2025

2007: 37 days median2008: 38 days median2011: 209 days median2014: 282 days median2015: 115 days median2016: 174 days median2017: 216 days median2018: 230 days median2019: 149 days median2020: 175 days median2022: 178 days median2023: 107 days median2025: 192 days median2026 (partial year): 180 days median
2007high 282 (2014) · low 37 (2007)2026

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

Recalls per year · EOB

1in 2023

2011: 22022: 12023: 12026 (partial year): 1
2007high 2 (2011) · low 0 (2007)2026

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

Adverse event reports per year · EOB

1,338in 2025

2007: 12008: 12009: 32011: 32012: 42013: 52014: 52015: 132016: 162017: 182018: 232019: 512020: 472021: 3452022: 1,1582023: 1,3522024: 1,4982025: 1,338
2007high 1,498 (2024) · low 0 (2010)2025

MAUDE reports naming product code EOB, 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
200743701
200843801
20091—03
20101—00
2011420923
20121—04
20130—05
2014328205
20153115013
20163174016
20176216018
20186230023
20198149051
20203175047
20212—0345
2022617811,158
2023310711,352
20242—01,498
2025319201,338
202651801—

What is it indicated for?

Smith & Nephew Images Endoscopic Video System and components are indicated for use in diagnostic and operative arthroscopic, laparoscopic and ENT endoscopic procedures to provide illumination and allow visualization of the surgical site.

Smith & Nephew Manual Surgical Instruments for Sinus Surgery are indicated for the endoscopic examination and treatment of the nasal cavity and nasal pharynx.

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. “K970247: Smith & Nephew Images Arthroscope/Ent Endoscope.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K970247

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