510(k) Report

510(k) · Cleared

Cleared

Perkinelmer XRD 1622 AP3 Med Flat Panel Detector

K122495510(k) TraditionalCleared Nov 28, 2012104-day reviewClass II21 CFR 892.1680

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

Perkinelmer, Inc. · MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)

Cleared on Nov 28, 2012 as substantially equivalent to K063283 (Sedecal., Sa., 2006) after a 104-day review. Its family tree reaches back 6 generations to 1998. 13 later devices descend from it.

Decided
Nov 28, 2012
Review
104 days
Class
Class II
Product code
MQB
Recalls
None
Predicates
1

Its longest line of descent runs back 6 generations to K981556 (1998). 13 ancestors in all, the oldest K862120 (1986). 13 later devices descend from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2006: 1 other ancestor2004: 1 other ancestor2001: 1 other ancestor1998: 1 other ancestor2002: 1 other ancestor2000: 1 other ancestor1986: 1 other ancestor2014: 2 descendants cleared2015: 1 descendant cleared2016: 2 descendants cleared2017: 1 descendant cleared2018: 1 descendant cleared2019: 1 descendant cleared2022: 1 descendant cleared2023: 1 descendant cleared2025: 1 descendant cleared2026: 2 descendants clearedK981556 · Canon X-Ray Digital Camera Cxdi-11 · Canon USA, Inc. · 1998K992547 · Canon X-Ray Digital Camera, Model Cxdi-22 · Canon USA, Inc. · 1999K023750 · Cannon Digital Radiography Model Cxdi-40G · Canon USA, Inc. · 2002K031447 · Canon, Digital Radiography, Model Cxdi-50G · Canon, Inc. · 2003K042876 · Urs LP Digital, Millennium, Radpro · Sedecal., Sa. · 2004K063283 · Definium 5000 X-Ray System · Sedecal., Sa. · 2006 · recalled1990200020102020
Other ancestors, by generationDescendants, by generation 2 generations back: 2 other ancestors3 generations back: 2 other ancestors4 generations back: 3 other ancestors 1 generation forward: 1 descendant2 generations forward: 5 descendants3 generations forward: 2 descendants4 generations forward: 1 descendant5 generations forward: 1 descendant6 generations forward: 2 descendants7 generations forward: 1 descendant K063283 · Definium 5000 X-Ray System · Sedecal., Sa. · 2006 · recalledK042876 · Urs LP Digital, Millennium, Radpro · Sedecal., Sa. · 2004K031447 · Canon, Digital Radiography, Model Cxdi-50G · Canon, Inc. · 2003K023750 · Cannon Digital Radiography Model Cxdi-40G · Canon USA, Inc. · 2002K992547 · Canon X-Ray Digital Camera, Model Cxdi-22 · Canon USA, Inc. · 1999K981556 · Canon X-Ray Digital Camera Cxdi-11 · Canon USA, Inc. · 1998−50+5
  1. Root · 6 generations backK981556 Canon X-Ray Digital Camera Cxdi-11Canon USA, Inc. · 1998
  2. 5 generations backK992547 Canon X-Ray Digital Camera, Model Cxdi-22Canon USA, Inc. · 1999
  3. 4 generations backK023750 Cannon Digital Radiography Model Cxdi-40GCanon USA, Inc. · 2002
  4. 3 generations backK031447 Canon, Digital Radiography, Model Cxdi-50GCanon, Inc. · 2003
  5. 2 generations backK042876 Urs LP Digital, Millennium, RadproSedecal., Sa. · 2004
  6. 1 generation backK063283 Definium 5000 X-Ray SystemSedecal., Sa. · 2006 · Recalled
  7. This deviceK122495 Perkinelmer XRD 1622 AP3 Med Flat Panel DetectorPerkinelmer, Inc. · 2012
  8. Descendant · cites it directly · 12 of its ownK140551 Perkinelmer, Xrpad 4336 Med Flat Panel DetectorPerkinelmer, Inc. · 2014
  9. Descendant · 2 generations on · 7 of its ownK142698 PerkinElmer, XRpad 4343 F MED Flat Panel DetectorPerkinelmer, Inc. · 2014
  10. Descendant · 2 generations on · 6 of its ownK162529 DigiX FDXAllengers Medical Systems Limited · 2017
  11. Descendant · 3 generations on · 5 of its ownK192541 DigiX FDXAllengers Medical Systems Limited · 2019
  12. Descendant · 4 generations on · 4 of its ownK223060 DigiX FDXAllengers Medical Systems Limited · 2022

Showing 5 of 13 descendants. See all descendants

Descendants cleared per year

2014: 22015: 12016: 22017: 12018: 12019: 12022: 12023: 12025: 12026: 2
2014high 2 (2014) · low 0 (2020)2026

Most influential descendants

Showing 5 of 13 · See all
  • K140551Perkinelmer, Xrpad 4336 Med Flat Panel DetectorPerkinelmer, Inc. · 2014 · cites it directly12descendants
  • K142698PerkinElmer, XRpad 4343 F MED Flat Panel DetectorPerkinelmer, Inc. · 2014 · 2 generations on7descendants
  • K162529DigiX FDXAllengers Medical Systems Limited · 2017 · 2 generations on6descendants
  • K192541DigiX FDXAllengers Medical Systems Limited · 2019 · 3 generations on5descendants
  • K223060DigiX FDXAllengers Medical Systems Limited · 2022 · 4 generations on4descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K981556Canon X-Ray Digital Camera Cxdi-11Canon USA, Inc.1998—
−5K992547Canon X-Ray Digital Camera, Model Cxdi-22Canon USA, Inc.1999—
−4K023750Cannon Digital Radiography Model Cxdi-40GCanon USA, Inc.2002—
−3K031447Canon, Digital Radiography, Model Cxdi-50GCanon, Inc.2003—
−2K042876Urs LP Digital, Millennium, RadproSedecal., Sa.2004—
−1K063283Definium 5000 X-Ray SystemSedecal., Sa.20063
0 (this device)K122495Perkinelmer XRD 1622 AP3 Med Flat Panel DetectorPerkinelmer, Inc.2012—
+1K140551Perkinelmer, Xrpad 4336 Med Flat Panel DetectorPerkinelmer, Inc.2014—
+2K142698PerkinElmer, XRpad 4343 F MED Flat Panel DetectorPerkinelmer, Inc.2014—
+2K162529DigiX FDXAllengers Medical Systems Limited2017—
+3K192541DigiX FDXAllengers Medical Systems Limited2019—
+4K223060DigiX FDXAllengers Medical Systems Limited2022—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198610
199810
200010
200110
200210
200410
200610

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201420
201510
201620
201710
201810
201910
202210
202310
202510
202620
FIG. 1 — Lineage of K122495, 1998–2026Source: 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 MQB? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new MQB device

  1. #1 K201528 Yushan X-Ray Flat Panel Detector with DROCscore 21.5 · 12 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

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
*K063283Definium 5000 X-Ray System
Summary page 1
…uct Code: (MQB) LO7.92(af3: Predicate device: Definium 5000 X-ray system (Flat Panel Detector in system) [K063283] 807.92(aK4-: Device Description: The XRD 1622 AP3 MED is a flat panel x-ray detector consisting of an amorphous silicon pa…
Sedecal., Sa.20063

What descends from it? (13)

See all 13

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

NumberDeviceApplicantDecidedDescendants
K140551Perkinelmer, Xrpad 4336 Med Flat Panel DetectorPerkinelmer, Inc.201412

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 14 years and passes through 4 companies; a new generation was cleared every 2.0 years on median.
  • 3 of the 13 ancestors have a recall of any class.
  • Of its descendants, K140551 (Perkinelmer, Inc., 2014) has gone furthest, with 12 descendants of its own.

How does its category compare?

All MQB devices

MQB Solid State X-Ray Imager (Flat Panel/Digital Imager): FDA decisions, review times, recalls and adverse event reports over 20 years. 2012, this device’s year, is highlighted.

FDA decisions per year · MQB

8in 2025

2007: 132008: 82009: 152010: 112011: 242012: 222013: 212014: 322015: 212016: 222017: 312018: 162019: 222020: 192021: 212022: 312023: 102024: 82025: 82026 (partial year): 3
2007high 32 (2014) · low 8 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MQB

127in 2025

2007: 22 days median2008: 15 days median2009: 57 days median2010: 116 days median2011: 102 days median2012: 80 days median2013: 105 days median2014: 102 days median2015: 81 days median2016: 92 days median2017: 30 days median2018: 30 days median2019: 30 days median2020: 28 days median2021: 48 days median2022: 48 days median2023: 30 days median2024: 187 days median2025: 127 days median2026 (partial year): 245 days median
2007high 245 (2026) · low 15 (2008)2026

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

Recalls per year · MQB

1in 2025

2007: 152008: 362009: 192010: 142011: 102012: 82013: 62017: 12018: 42019: 12020: 42021: 12025: 12026 (partial year): 1
2007high 36 (2008) · low 0 (2014)2026

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

Adverse event reports per year · MQB

141in 2025

2007: 252008: 302009: 342010: 392011: 1012012: 2672013: 1592014: 292015: 212016: 262017: 202018: 842019: 452020: 92021: 262022: 132023: 512024: 912025: 141
2007high 267 (2012) · low 9 (2020)2025

MAUDE reports naming product code MQB, 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
200713221525
20088153630
200915571934
2010111161439
20112410210101
201222808267
2013211056159
201432102029
20152181021
20162292026
20173130120
20181630484
20192230145
2020192849
20212148126
20223148013
20231030051
20248187091
202581271141
202632451—

What is it indicated for?

The XRD 1622 AP3 MED, when used with a radiographic imaging system, is indicated for use in generating radiographic images of human anatomy for diagnostic X-ray procedures, wherever conventional screen-film (SF), digital radiography (DR), or computed radiography (CR) systems may be used. It is not intended for mammographic use.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K122495: Perkinelmer XRD 1622 AP3 Med Flat Panel Detector.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K122495

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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