510(k) Report

510(k) · Cleared

Cleared

NP-2600 Series Hardcopy Printers

K042232510(k) TraditionalCleared Oct 5, 200449-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

Codonics, Inc. · LMC Camera, Multi Format, Radiological

Cleared on Oct 5, 2004 as substantially equivalent to K003481 (Codonics, Inc., 2001) and 3 other predicates after a 49-day review. Its family tree reaches back 3 generations to 2000. 1 later device descends from it.

Decided
Oct 5, 2004
Review
49 days
Class
Class II
Product code
LMC
Recalls
None
Predicates
4

Its longest line of descent runs back 3 generations to K002146 (2000). 9 ancestors in all, the oldest K962364 (1996). 1 later device descends from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2003: 1 other ancestor2001: 2 other ancestors1999: 1 other ancestor1997: 1 other ancestor1996: 1 other ancestor2009: 1 descendant clearedK002146 · Kodak Dryview 8610 Laser Imager / for Mammography · Eastman Kodak Company · 2000K012941 · Drystar, Model 4500M · Agfa Corp. · 2001K021054 · Codonics Horizon CI Medical Multimedia Dry Imager; Codonics Horizon GS Medical Multimedia Grey Scale Dry Imager · Codonics, Inc. · 20021995200020052010201520202025
Other ancestors, by generationDescendants, by generation 1 generation back: 3 other ancestors2 generations back: 2 other ancestors3 generations back: 1 other ancestor 1 generation forward: 1 descendant K021054 · Codonics Horizon CI Medical Multimedia Dry Imager; Codonics Horizon GS Medical Multimedia Grey Scale Dry Imager · Codonics, Inc. · 2002K012941 · Drystar, Model 4500M · Agfa Corp. · 2001K002146 · Kodak Dryview 8610 Laser Imager / for Mammography · Eastman Kodak Company · 20000
  1. Root · 3 generations backK002146 Kodak Dryview 8610 Laser Imager / for MammographyEastman Kodak Company · 2000
  2. 2 generations backK012941 Drystar, Model 4500MAgfa Corp. · 2001
  3. 1 generation backK021054 Codonics Horizon CI Medical Multimedia Dry Imager; Codonics Horizon…Codonics, Inc. · 2002
  4. This deviceK042232 NP-2600 Series Hardcopy PrintersCodonics, Inc. · 2004
  5. Descendant · cites it directly · 0 of its ownK092280 Cypher Dicom Print SolutionVirtual Imaging, Inc. · 2009

Most influential descendants

Showing 1 of 1 · See all
  • K092280Cypher Dicom Print SolutionVirtual Imaging, Inc. · 2009 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K002146Kodak Dryview 8610 Laser Imager / for MammographyEastman Kodak Company2000—
−2K012941Drystar, Model 4500MAgfa Corp.2001—
−1K021054Codonics Horizon CI Medical Multimedia Dry Imager; Codonics Horizon GS Medical…Codonics, Inc.2002—
0 (this device)K042232NP-2600 Series Hardcopy PrintersCodonics, Inc.2004—
+1K092280Cypher Dicom Print SolutionVirtual Imaging, Inc.2009—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199610
199710
199910
200120
200310

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200910
FIG. 1 — Lineage of K042232, 2000–2009Source: 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 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? (4)

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
*K003481Codonics NP-1660 Series Medical Printers, Model 1660
Summary page 1
…ies Medical Dry Imagers 2.5 Predicate Devices: Codonics NP-i1 660 Series Medical Printers (Premarket notification K003481'j, Codonics Horizon Series Medical Hardcopy Dry Imagers (Premarket notification K021054),…
Codonics, Inc.2001—
*K021054Codonics Horizon CI Medical Multimedia Dry Imager; Codonics Horizon GS Medical…
Summary page 1
…notification K003481'j, Codonics Horizon Series Medical Hardcopy Dry Imagers (Premarket notification K021054), Codonics EP-1000 Medical Image Hardcopy Color Printers…
Codonics, Inc.2002—
*K030690Codonics EP-1000 Medical Color Dry Imagers
Summary page 1
…on K021054), Codonics EP-1000 Medical Image Hardcopy Color Printers (premarket notification K030690) and the Seiko ColorPoint 1720 (Premarket notification K991 282) 3 Device Description…
Codonics, Inc.2003—
*K991282Colorpoint 1720 Medical Imagers and Video Capture Box CX-1000 Series
Summary page 1
…ters (premarket notification K030690) and the Seiko ColorPoint 1720 (Premarket notification K991 282) 3 Device Description 807.92(a)(4) 3.1 Function The NP-2600 Series Imagers are dry, therm…
Seiko Instruments USA, Inc.1999—

Also cleared against K003481: 1 other device →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K092280Cypher Dicom Print SolutionVirtual Imaging, Inc.20090

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 4 years and passes through 3 companies; a new generation was cleared every 1.2 years on median.
  • None of the 9 ancestors has a recall.
  • Of its descendants, K092280 (Virtual Imaging, Inc., 2009) has gone furthest, with 0 descendants of its own.
  • 1 other device also cites its predicate K003481.

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 intended uses of the NP-2600 Series Imagers is high resolution hard copy imaging of digital image source material and through the conversion of electronic signals from a wide variety of direct/indirect medical imaging modality outputs. The hardcopy output includes however is not limited to, digital radiography, nuclear medicine, ultrasound, CT, MRI, CR and Radiation Therapy planning; however, does not include digital mammography hardcopy. Images are…

Read the full statement (150 words)

The intended uses of the NP-2600 Series Imagers is high resolution hard copy imaging of digital image source material and through the conversion of electronic signals from a wide variety of direct/indirect medical imaging modality outputs. The hardcopy output includes however is not limited to, digital radiography, nuclear medicine, ultrasound, CT, MRI, CR and Radiation Therapy planning; however, does not include digital mammography hardcopy. Images are suitable for medical image diagnosis use and referral. The system is intended for use by medical radiologists, imaging modality specialists, and communications to referring physicians.

The intended uses are essentially identical to the Codonics NP-1660 Series Medical Printers (Premarket notification K003481), the Codonics Horizon Series Medical Hardcopy Dry Imagers (Premarket notification K021054). The intended uses are identical to the Codonics EP-1000 Medical Image Hardcopy Color Printers (Premarket notification K030690) and the Seiko ColorPoint 1720 (Premarket notification K991282) in terms of color, reflective media output.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K042232: NP-2600 Series Hardcopy Printers.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K042232

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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