510(k) Report

510(k) · Cleared

Cleared

Konica Laser Imager, Drypro Model 722

K992586510(k) TraditionalCleared Oct 29, 199988-day reviewClass II21 CFR 892.2040

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

Konica Corp. · LMC Camera, Multi Format, Radiological

Cleared on Oct 29, 1999 after an 88-day review. FDA’s file for it is a 510(k) statement, which names no predicate. 1 later device descends from it.

Decided
Oct 29, 1999
Review
88 days
Class
Class II
Product code
LMC
Recalls
None
Predicates
0

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

Descendants, by year cleared 2002: 1 descendant cleared1995200020052010201520202025
  1. This deviceK992586 Konica Laser Imager, Drypro Model 722Konica Corp. · 1999
  2. Descendant · cites it directly · 0 of its ownK013052 Konica Laser Imager, Drypro Model 751/752Konica Minolta Medical & Graphic, Inc. · 2002

Most influential descendants

Showing 1 of 1 · See all
  • K013052Konica Laser Imager, Drypro Model 751/752Konica Minolta Medical & Graphic, Inc. · 2002 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K992586Konica Laser Imager, Drypro Model 722Konica Corp.1999—
+1K013052Konica Laser Imager, Drypro Model 751/752Konica Minolta Medical & Graphic, Inc.2002—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200210
FIG. 1 — Lineage of K992586, 1999–2002Source: 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), the FDA 510(k) statement (indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in LMC? 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’s file for it is a 510(k) statement, which names no predicate.

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K013052Konica Laser Imager, Drypro Model 751/752Konica Minolta Medical & Graphic, Inc.20020

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, K013052 (Konica Minolta Medical & Graphic, Inc., 2002) has gone furthest, with 0 descendants of its own.

How does its category compare?

All LMC devices

LMC Camera, Multi Format, Radiological: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · LMC

2in 2014

2007: 12008: 12009: 32011: 12014: 2
2007high 3 (2009) · low 0 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LMC

80in 2009

2009: 80 days median
2007high 80 (2009)2026

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

Recalls per year · LMC

1in 2008

2008: 1
2007high 1 (2008) · low 0 (2007)2026

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

Adverse event reports per year · LMC

2in 2018

2013: 12014: 12018: 2
2007high 2 (2018) · low 0 (2007)2025

MAUDE reports naming product code LMC, 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—00
20081—10
200938000
20100—00
20111—00
20120—00
20130—01
20142—01
20150—00
20160—00
20170—00
20180—02
20190—00
20200—00
20210—00
20220—00
20230—00
20240—00
20250—00
20260—0—

What is it indicated for?

The Konica Laser Imager DRYPRO model 722 is a laser imager converts data from diagnostic equipment such as CT, MRI, DSA, and other medical devices into various intensities, scan and then print the data onto laser imaging film.

Indications for use read by OCR from a scanned FDA 510(k) statement, so letters may be misread. Check the PDF before quoting it.

More from Konica Corp.

5 FDA decisions under this applicant name. See the company

  • K990359Konica Direct Digitizer, Model DD-341Konica Corp. · 1999
  • K980873Konica Direct Digitizer Regius Model 330Konica Corp. · 1998
  • K920769Konica LI 10 and 10A Laser ImagerKonica Corp. · 1992
  • K920558Konica Direct Digitizer KD-1000Konica Corp. · 1992

Recent decisions in LMC

The LMC category page

  • K141454Sony Digital Printer UP-D898MD/Sony Hybrid Printer UP-X898MDSony Electronics, Inc. · 2014
  • K141346Sony Hybird Graphic UP-971AD, Sony Hybird Graphic Printer UP-991ADSony Electronics, Inc. · 2014
  • K111566Dryview Chroma Imaging SystemCarestream Health, Inc. · 2011
  • K092280Cypher Dicom Print SolutionVirtual Imaging, Inc. · 2009
  • K090469Carestream Dryview 5850 Laser ImagerCarestream Health, Inc. · 2009

https://510kreport.com/device/K992586 · printed Nov 4, 2026

Cite this page

510(k) Report. “K992586: Konica Laser Imager, Drypro Model 722.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K992586

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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