510(k) Report

510(k) · Cleared

Cleared

KY-M280U Surgical Camera

K854988510(k) TraditionalCleared Jan 24, 198643-day reviewClass I21 CFR 878.4160

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

Us Jvc Corp. · FWC Camera, Television, Surgical, With Audio

Cleared on Jan 24, 1986 after a 43-day review. FDA has not posted a summary or statement for it, so its predicates are not known.

Decided
Jan 24, 1986
Review
43 days
Class
Class I
Product code
FWC
Recalls
None
Predicates
0

FDA has not posted a summary or statement for it, so its predicates are not known.

FIG. 1 — Lineage of K854988Source: 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), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in FWC? 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?

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 FWC devices

FWC Camera, Television, Surgical, With Audio: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · FWC

FDA has decided no FWC device since 2007.

Median 510(k) review, days · FWC

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

Recalls per year · FWC

No recall names FWC since 2007.

Adverse event reports per year · FWC

7in 2025

2012: 12015: 12016: 12018: 52019: 12020: 42021: 222022: 172023: 102024: 52025: 7
2007high 22 (2021) · low 0 (2007)2025

MAUDE reports naming product code FWC, 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—00
20080—00
20090—00
20100—00
20110—00
20120—01
20130—00
20140—00
20150—01
20160—01
20170—00
20180—05
20190—01
20200—04
20210—022
20220—017
20230—010
20240—05
20250—07
20260—0—
Cite this page

510(k) Report. “K854988: KY-M280U Surgical Camera.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K854988

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Record history
  • FDA decision record loaded May 2, 2026
  • Page last updated Nov 3, 2026