510(k) · Cleared
ClearedNew Detector for Transcam/Polaris S315
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Adac Laboratories · IYX Camera, Scintillation (Gamma)
Cleared on Jan 15, 1993 after a 135-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 4 later devices descend from it.
- Decided
- Jan 15, 1993
- Review
- 135 days
- Class
- Class I
- Product code
- IYX
- Recalls
- None
- Predicates
- 0
4 later devices descend from it, 1 citing it directly.
- This deviceK924639 New Detector for Transcam/Polaris S315Adac Laboratories · 1993
- Descendant · cites it directly · 3 of its ownK984466 Dilon 2000, Model 2000-6X8 and Dilon 2000, Model 2000-5X5Dilon Technologies, Inc. · 1999
- Descendant · 2 generations on · 1 of its ownK082588 Gammaloc System, Model 03-00001Dilon Technologies, LLC · 2009
- Descendant · 3 generations on · 0 of its ownK160933 Discovery NM 750b BopsyGE Healthcare · 2016
- Descendant · 2 generations on · 0 of its ownK110384 Dilon 6800 Acella (Acella)Dilon Technologies, Inc. · 2011
Most influential descendants
Showing 4 of 4 · See all- K984466Dilon 2000, Model 2000-6X8 and Dilon 2000, Model 2000-5X5Dilon Technologies, Inc. · 1999 · cites it directly3descendants
- K082588Gammaloc System, Model 03-00001Dilon Technologies, LLC · 2009 · 2 generations on1descendant
- K160933Discovery NM 750b BopsyGE Healthcare · 2016 · 3 generations on0descendants
- K110384Dilon 6800 Acella (Acella)Dilon Technologies, Inc. · 2011 · 2 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K924639 | New Detector for Transcam/Polaris S315 | Adac Laboratories | 1993 | — |
| +1 | K984466 | Dilon 2000, Model 2000-6X8 and Dilon 2000, Model 2000-5X5 | Dilon Technologies, Inc. | 1999 | — |
| +2 | K082588 | Gammaloc System, Model 03-00001 | Dilon Technologies, LLC | 2009 | — |
| +3 | K160933 | Discovery NM 750b Bopsy | GE Healthcare | 2016 | — |
| +2 | K110384 | Dilon 6800 Acella (Acella) | Dilon Technologies, Inc. | 2011 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1999 | 1 | 0 |
| 2009 | 1 | 0 |
| 2011 | 1 | 0 |
| 2016 | 1 | 0 |
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 IYX? 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 IYX device
- #1 K230221 QDOSE® Multi-purpose Voxel Dosimetry…score 6.2 · 2 generations · no Class I recall
- #2 Held for the reportin the 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? (4)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K984466 | Dilon 2000, Model 2000-6X8 and Dilon 2000, Model 2000-5X5 | 1999 | 3 |
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, K984466 (Dilon Technologies, Inc., 1999) has gone furthest, with 3 descendants of its own.
How does its category compare?
All IYX devicesIYX Camera, Scintillation (Gamma): FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · IYX
2in 2023
2026 to Oct 25, outlined.
Median 510(k) review, days · IYX
82in 2011
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · IYX
2in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · IYX
1in 2022
MAUDE reports naming product code IYX, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 2 | — | 0 | 11 |
| 2008 | 2 | — | 0 | 10 |
| 2009 | 2 | — | 0 | 8 |
| 2010 | 4 | 82 | 0 | 5 |
| 2011 | 3 | 82 | 0 | 6 |
| 2012 | 0 | — | 0 | 1 |
| 2013 | 1 | — | 0 | 1 |
| 2014 | 1 | — | 0 | 3 |
| 2015 | 0 | — | 0 | 4 |
| 2016 | 2 | — | 0 | 2 |
| 2017 | 1 | — | 0 | 0 |
| 2018 | 0 | — | 0 | 1 |
| 2019 | 0 | — | 0 | 0 |
| 2020 | 0 | — | 0 | 0 |
| 2021 | 0 | — | 0 | 0 |
| 2022 | 0 | — | 0 | 1 |
| 2023 | 2 | — | 0 | 0 |
| 2024 | 0 | — | 0 | 0 |
| 2025 | 0 | — | 2 | 0 |
| 2026 | 0 | — | 0 | — |
https://510kreport.com/device/K924639 · printed Nov 6, 2026
Cite this page
510(k) Report. “K924639: New Detector for Transcam/Polaris S315.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K924639
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Record history
- FDA decision record loaded May 2, 2026
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026