510(k) · Cleared
ClearedCellvizio 100 Series System with Confocal Miniprobes (TM)
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Mauna Kea Technologies · OWN Confocal Optical Imaging
Cleared on Jul 25, 2014 as substantially equivalent to K111047 (Mauna Kea Technologies, Inc., 2011) and 1 other predicate after a 255-day review. Its family tree reaches back 6 generations to 1993. 1 of the 30 devices in its family, counting itself, has a Class I recall. 7 later devices descend from it.
- Decided
- Jul 25, 2014
- Review
- 255 days
- Class
- Class II
- Product code
- OWN
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 6 generations to K926514 (1993). 22 ancestors in all, the oldest K822846 (1982). 7 later devices descend from it, 1 citing it directly. 1 of the 30 devices in this family, counting this one, has a Class I recall.
- Root · 6 generations backK926514 Endoscopic Ultrasound System Type 20Olympus Corp. · 1993 · Recalled
- 5 generations backK951994 Olympus EU-M30 Endoscopic Ultrasound CenterOlympus America, Inc. · 1996
- 4 generations backK982323 Olympus UM 2R/3R Ultrasonic Probes and Associated Ancillary…Olympus America, Inc. · 1998
- 3 generations backK042438 Superdimension/BronchusSuperdimension, Ltd. · 2004 · Recalled
- 2 generations backK051585 F-400 SystemMauna Kea Technologies · 2005
- 1 generation backK111047 Cellvizio 100 Series System with Confocal MiniprobesMauna Kea Technologies, Inc. · 2011
- This deviceK133466 Cellvizio 100 Series System with Confocal Miniprobes (TM)Mauna Kea Technologies · 2014
- Descendant · cites it directly · 6 of its ownK172844 Cellvizio 100 Series System with Confocal MiniprobesMauna Kea Technologies · 2017
- Descendant · 2 generations on · 4 of its ownK183640 Cellvizio 100 Series Confocal laser Imaging systems and their…Mauna Kea Technologies · 2019
- Descendant · 2 generations on · 2 of its ownK191144 Cellvizio 100 Series System with Confocal MiniprobesMauna Kea Technologies · 2020
- Descendant · 3 generations on · 0 of its ownK243711 Confocal Microprobe Imaging System (BrightP980); Confocal Microprobe…Wuxi Hisky Medical Technologies Co., Ltd. · 2025
- Descendant · 3 generations on · 0 of its ownK241275 Histolog® Scanner (Hardware 2.4, Software 3.3)Samantree Medical SA · 2024
Showing 5 of 7 descendants. See all descendants
Descendants cleared per year
Class I recalls in this family
- K023984 Modification to Olympus Bronchoscopes BF-40…3 generations back · 2003
Most influential descendants
Showing 5 of 7 · See all- K172844Cellvizio 100 Series System with Confocal MiniprobesMauna Kea Technologies · 2017 · cites it directly6descendants
- K183640Cellvizio 100 Series Confocal laser Imaging systems and their Confocal MiniprobesMauna Kea Technologies · 2019 · 2 generations on4descendants
- K191144Cellvizio 100 Series System with Confocal MiniprobesMauna Kea Technologies · 2020 · 2 generations on2descendants
- K243711Confocal Microprobe Imaging System (BrightP980); Confocal Microprobe Imaging System…Wuxi Hisky Medical Technologies Co., Ltd. · 2025 · 3 generations on0descendants
- K241275Histolog® Scanner (Hardware 2.4, Software 3.3)Samantree Medical SA · 2024 · 3 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −6 | K926514 | Endoscopic Ultrasound System Type 20 | Olympus Corp. | 1993 | 1 |
| −5 | K951994 | Olympus EU-M30 Endoscopic Ultrasound Center | Olympus America, Inc. | 1996 | — |
| −4 | K982323 | Olympus UM 2R/3R Ultrasonic Probes and Associated Ancillary Equipment, for… | Olympus America, Inc. | 1998 | — |
| −3 | K042438 | Superdimension/Bronchus | Superdimension, Ltd. | 2004 | 1 |
| −2 | K051585 | F-400 System | Mauna Kea Technologies | 2005 | — |
| −1 | K111047 | Cellvizio 100 Series System with Confocal Miniprobes | Mauna Kea Technologies, Inc. | 2011 | — |
| 0 (this device) | K133466 | Cellvizio 100 Series System with Confocal Miniprobes (TM) | Mauna Kea Technologies | 2014 | — |
| +1 | K172844 | Cellvizio 100 Series System with Confocal Miniprobes | Mauna Kea Technologies | 2017 | — |
| +2 | K183640 | Cellvizio 100 Series Confocal laser Imaging systems and their Confocal… | Mauna Kea Technologies | 2019 | — |
| +2 | K191144 | Cellvizio 100 Series System with Confocal Miniprobes | Mauna Kea Technologies | 2020 | — |
| +3 | K243711 | Confocal Microprobe Imaging System (BrightP980); Confocal Microprobe Imaging… | Wuxi Hisky Medical Technologies Co., Ltd. | 2025 | — |
| +3 | K241275 | Histolog® Scanner (Hardware 2.4, Software 3.3) | Samantree Medical SA | 2024 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1982 | 1 | 0 |
| 1988 | 1 | 0 |
| 1991 | 2 | 0 |
| 1993 | 1 | 0 |
| 1994 | 2 | 0 |
| 1995 | 1 | 0 |
| 1996 | 2 | 0 |
| 2000 | 1 | 0 |
| 2002 | 1 | 0 |
| 2003 | 1 | 1 |
| 2004 | 2 | 0 |
| 2006 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2017 | 1 | 0 |
| 2019 | 1 | 0 |
| 2020 | 2 | 0 |
| 2021 | 1 | 0 |
| 2024 | 1 | 0 |
| 2025 | 1 | 0 |
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.
1 device in this family has a Class I recall. 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 OWN device
- #1 K231854 1788 4K Camera System with Advanced Imaging…score 24.9 · 24 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (2)
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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K111047 | Cellvizio 100 Series System with Confocal MiniprobesSummary page 1…OWN / 21 CFR 876.1500 Classification: Class 11 Predicate Device(s) [807.92(a)(3)]: *Cellvizio® 100 Series System with Confocal Miniprobes TM (K1 11047) *Celivizie® (-GI, -Lung) with Confocal Miniprobe TM (K061666) Device Description: [807.92(a)(4)]: t he subject device, "… | 2011 |
| * | K061666 | Cellvizio with Confocal Miniprobes, Model F-600; Coloflex and GastroflexSummary page 1…Predicate Device(s) [807.92(a)(3)]: *Cellvizio® 100 Series System with Confocal Miniprobes TM (K1 11047) *Celivizie® (-GI, -Lung) with Confocal Miniprobe TM (K061666) Device Description: [807.92(a)(4)]: t he subject device, "Cellvizic® 100 Series F700-v2 system with Confocal Miniprobes" opera… | 2006 |
What descends from it? (7)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K172844 | Cellvizio 100 Series System with Confocal Miniprobes | 2017 | 6 |
Has anything in its family been recalled? (1 Class I)
No FDA recall names this device.
Relatives with a Class I recall
Class I is FDA’s most serious recall class. A recall in the family tree is context for this device, not evidence about it.
- K023984Modification to Olympus Bronchoscopes BF-40 Series, BF-240 Series, and BF-160 SeriesThe Olympus Optical Co. · 2003 · 3 generations back · ◆ in the 2003 ancestors bar of FIG. 114 Class I recalls
What does this lineage say?
- The line of descent spans 21 years and passes through 5 companies; a new generation was cleared every 3.0 years on median.
- 7 of the 22 ancestors have a recall of any class; 1 has a Class I recall.
- Of its descendants, K172844 (Mauna Kea Technologies, 2017) has gone furthest, with 6 descendants of its own.
- 4 other devices also cite its predicate K111047.
How does its category compare?
All OWN devicesOWN Confocal Optical Imaging: FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, this device’s year, is highlighted.
FDA decisions per year · OWN
3in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · OWN
196in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · OWN
1in 2024
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · OWN
197in 2025
MAUDE reports naming product code OWN, 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 | 0 | — | 0 | 0 |
| 2008 | 0 | — | 0 | 0 |
| 2009 | 0 | — | 0 | 0 |
| 2010 | 0 | — | 0 | 0 |
| 2011 | 1 | — | 0 | 0 |
| 2012 | 3 | 87 | 0 | 0 |
| 2013 | 2 | — | 0 | 0 |
| 2014 | 5 | 208 | 0 | 0 |
| 2015 | 5 | 163 | 0 | 1 |
| 2016 | 2 | — | 0 | 4 |
| 2017 | 5 | 87 | 0 | 12 |
| 2018 | 1 | — | 0 | 11 |
| 2019 | 7 | 81 | 0 | 59 |
| 2020 | 7 | 81 | 0 | 105 |
| 2021 | 4 | 104 | 0 | 312 |
| 2022 | 4 | 41 | 3 | 346 |
| 2023 | 6 | 69 | 0 | 164 |
| 2024 | 1 | — | 1 | 165 |
| 2025 | 3 | 196 | 0 | 197 |
| 2026 | 7 | 63 | 0 | — |
What is it indicated for?
The Cellvizio® 100 Series system with Confocal Miniprobes is a confocal laser system with fiber optic probes that is intended to allow imaging of the internal microstructure of tissues in anatomical tracts, i.e., gastrointestinal or respiratory, accessed by an endoscope or endoscopic accessories.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K133466 · printed Nov 6, 2026
Cite this page
510(k) Report. “K133466: Cellvizio 100 Series System with Confocal Miniprobes (TM).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K133466
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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