510(k) Report

510(k) · Cleared

Cleared

Wise Image Management System

K971451510(k) TraditionalCleared Jun 26, 199766-day reviewClass I21 CFR 892.2010

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

O Tech, Inc. · LMB Device, Digital Image Storage, Radiological

Cleared on Jun 26, 1997 as substantially equivalent to K963395 (Sectra-Imtec AB, 1996) after a 66-day review. Its family tree reaches back 2 generations to 1993. 2 later devices descend from it.

Decided
Jun 26, 1997
Review
66 days
Class
Class I
Product code
LMB
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K922164 (1993). 2 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 1998: 1 descendant cleared1999: 1 descendant clearedK922164 · Raytel Digital Imaging Systems · Olicon Imaging Systems, Inc. · 1993K963395 · Imageserver 2000 Picture Archiving System · Sectra-Imtec AB · 19961990200020102020
Descendants, by generation 1 generation forward: 1 descendant2 generations forward: 1 descendant K963395 · Imageserver 2000 Picture Archiving System · Sectra-Imtec AB · 1996K922164 · Raytel Digital Imaging Systems · Olicon Imaging Systems, Inc. · 19930
  1. Root · 2 generations backK922164 Raytel Digital Imaging SystemsOlicon Imaging Systems, Inc. · 1993
  2. 1 generation backK963395 Imageserver 2000 Picture Archiving SystemSectra-Imtec AB · 1996
  3. This deviceK971451 Wise Image Management SystemO Tech, Inc. · 1997
  4. Descendant · cites it directly · 1 of its ownK983447 Wise (II) Image Management SystemSectra-Imtec AB · 1998 · Recalled
  5. Descendant · 2 generations on · 0 of its ownK992426 Raypax Web Clinical SystemSamsung Sds Co., Ltd. · 1999

Most influential descendants

Showing 2 of 2 · See all
  • K983447Wise (II) Image Management SystemSectra-Imtec AB · 1998 · cites it directly1descendant
  • K992426Raypax Web Clinical SystemSamsung Sds Co., Ltd. · 1999 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K922164Raytel Digital Imaging SystemsOlicon Imaging Systems, Inc.1993—
−1K963395Imageserver 2000 Picture Archiving SystemSectra-Imtec AB1996—
0 (this device)K971451Wise Image Management SystemO Tech, Inc.1997—
+1K983447Wise (II) Image Management SystemSectra-Imtec AB19983
+2K992426Raypax Web Clinical SystemSamsung Sds Co., Ltd.1999—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199810
199910
FIG. 1 — Lineage of K971451, 1993–1999Source: 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.

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  • 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? (1)

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
*K963395Imageserver 2000 Picture Archiving System
Summary page 1
…otification for the above referenced product contains adequate information and data to enable CDRH to determine substantial equivalence to SECTRA-Imtec ImageServer 2000 (K963395). This information and data is summarised as follows: 1. WISE is subject to and in compliance with the Federal Performance Stand…
Sectra-Imtec AB1996—

Also cleared against K963395: 1 other device →

What descends from it? (2)

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

NumberDeviceApplicantDecidedDescendants
K983447Wise (II) Image Management SystemSectra-Imtec AB19981

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 3.8 years on median.
  • None of the 2 ancestors has a recall.
  • Of its descendants, K983447 (Sectra-Imtec AB, 1998) has gone furthest, with 1 descendant of its own.
  • 1 other device also cites its predicate K963395.

How does its category compare?

All LMB devices

LMB Device, Digital Image Storage, Radiological: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · LMB

FDA has decided no LMB device since 2007.

Median 510(k) review, days · LMB

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

Recalls per year · LMB

1in 2013

2008: 12009: 52011: 22013: 1
2007high 5 (2009) · low 0 (2007)2026

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

Adverse event reports per year · LMB

7in 2025

2007: 12008: 32009: 32010: 162011: 42012: 42013: 72014: 12016: 212017: 102018: 52019: 102020: 82021: 102023: 102024: 92025: 7
2007high 21 (2016) · low 0 (2015)2025

MAUDE reports naming product code LMB, 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—01
20080—13
20090—53
20100—016
20110—24
20120—04
20130—17
20140—01
20150—00
20160—021
20170—010
20180—05
20190—010
20200—08
20210—010
20220—00
20230—010
20240—09
20250—07
20260—0—

What is it indicated for?

The SECTRA AB, WISE Image Management System device is intended for the management and displaying of x-ray images, other radiological objects, and information.

It can manage images from different modalities, single and multiple file servers, and interfaces to various Radiological Information Systems (RIS), image storage and printing devices using DICOM or similar interface standards.

Typical users of this system are trained professionals, including but not limited to physicians, radiologists, nurses, medical technicians, and assistants,

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. “K971451: Wise Image Management System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K971451

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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