510(k) Report

510(k) · Cleared

Cleared

Sony Video Printers, UP Series

K882958510(k) TraditionalCleared Aug 4, 198821-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

Sony Medical Electronics Co. · KQM Camera, Surgical And Accessories

Cleared on Aug 4, 1988 after a 21-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it.

Decided
Aug 4, 1988
Review
21 days
Class
Class I
Product code
KQM
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 2014: 1 descendant cleared1990200020102020
  1. This deviceK882958 Sony Video Printers, UP SeriesSony Medical Electronics Co. · 1988
  2. Descendant · cites it directly · 0 of its ownK141346 Sony Hybird Graphic UP-971AD, Sony Hybird Graphic Printer UP-991ADSony Electronics, Inc. · 2014

Most influential descendants

Showing 1 of 1 · See all
  • K141346Sony Hybird Graphic UP-971AD, Sony Hybird Graphic Printer UP-991ADSony Electronics, Inc. · 2014 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K882958Sony Video Printers, UP SeriesSony Medical Electronics Co.1988—
+1K141346Sony Hybird Graphic UP-971AD, Sony Hybird Graphic Printer UP-991ADSony Electronics, Inc.2014—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201410
FIG. 1 — Lineage of K882958, 1988–2014Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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 KQM? 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
Get a 510(k) Report

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? (1)

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

NumberDeviceApplicantDecidedDescendants
K141346Sony Hybird Graphic UP-971AD, Sony Hybird Graphic Printer UP-991ADSony Electronics, Inc.20140

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?

  • Of its descendants, K141346 (Sony Electronics, Inc., 2014) has gone furthest, with 0 descendants of its own.

How does its category compare?

All KQM devices

KQM Camera, Surgical And Accessories: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · KQM

FDA has decided no KQM device since 2007.

Median 510(k) review, days · KQM

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

Recalls per year · KQM

1in 2023

2007: 12010: 72015: 12023: 1
2007high 7 (2010) · low 0 (2008)2026

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

Adverse event reports per year · KQM

9in 2025

2007: 12011: 22012: 42013: 32014: 62015: 72016: 112017: 52018: 92019: 62020: 192021: 92022: 62023: 102024: 292025: 9
2007high 29 (2024) · low 0 (2008)2025

MAUDE reports naming product code KQM, 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—11
20080—00
20090—00
20100—70
20110—02
20120—04
20130—03
20140—06
20150—17
20160—011
20170—05
20180—09
20190—06
20200—019
20210—09
20220—06
20230—110
20240—029
20250—09
20260—0—
Cite this page

510(k) Report. “K882958: Sony Video Printers, UP Series.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K882958

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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