510(k) · Cleared
ClearedEndoscopic Insufflation Unit, Model Xecr-2
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Olympus Medical Systems Corporation · FCX Insufflator, Automatic Carbon-Dioxide For Endoscope
Cleared on Mar 5, 2007 as substantially equivalent to K881004 (Keymed, Inc., 1988) and 1 other predicate after a 74-day review. Its family tree reaches back 1 generation to 1988. 2 later devices descend from it.
- Decided
- Mar 5, 2007
- Review
- 74 days
- Class
- Class II
- Product code
- FCX
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 1 generation to K881004 (1988). 2 ancestors in all. 2 later devices descend from it, 1 citing it directly.
- Root · 1 generation backK881004 Olympus-Keymed Endoscopic CO2 Regulator, Model EcrKeymed, Inc. · 1988
- This deviceK063786 Endoscopic Insufflation Unit, Model Xecr-2Olympus Medical Systems Corporation · 2007
- Descendant · cites it directly · 1 of its ownK133976 Fujifilm Endoscopic CO2 RegulatorFujifilm Medical System U.S.A., Inc. · 2014
- Descendant · 2 generations on · 0 of its ownK180711 FUJIFILM Endoscopic CO2 Regulator GW-100Fujifilm Corporation · 2018
Most influential descendants
Showing 2 of 2 · See allView FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K881004 | Olympus-Keymed Endoscopic CO2 Regulator, Model Ecr | Keymed, Inc. | 1988 | — |
| 0 (this device) | K063786 | Endoscopic Insufflation Unit, Model Xecr-2 | Olympus Medical Systems Corporation | 2007 | — |
| +1 | K133976 | Fujifilm Endoscopic CO2 Regulator | Fujifilm Medical System U.S.A., Inc. | 2014 | — |
| +2 | K180711 | FUJIFILM Endoscopic CO2 Regulator GW-100 | Fujifilm Corporation | 2018 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2005 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2014 | 1 | 0 |
| 2018 | 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.
Planning a device in FCX? 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 FCX device
- #1 K262152 VS-370CF, VS-370CTscore 15.3 · 13 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 |
|---|---|---|---|
| * | K881004 | Olympus-Keymed Endoscopic CO2 Regulator, Model EcrSummary page 2…n Name Endoscopic Insufflator Endoscopic Insufflator Manufacturer KeyMed, Ltd. E-Z-EM, Inc. 510(k) No. K881004 K053008 4 Device Description The Endoscopic Insufflation Unit model XECR-2 is used to dist… | 1988 |
| * | K053008 | E-Z-EM Endoscopic CO2 RegulatorSummary page 2…Endoscopic Insufflator Manufacturer KeyMed, Ltd. E-Z-EM, Inc. 510(k) No. K881004 K053008 4 Device Description The Endoscopic Insufflation Unit model XECR-2 is used to distend the gastrointestinal tract to opti… | 2005 |
What descends from it? (2)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K133976 | Fujifilm Endoscopic CO2 Regulator | 2014 | 1 |
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?
- None of the 2 ancestors has a recall.
- Of its descendants, K133976 (Fujifilm Medical System U.S.A., Inc., 2014) has gone furthest, with 1 descendant of its own.
How does its category compare?
All FCX devicesFCX Insufflator, Automatic Carbon-Dioxide For Endoscope: FDA decisions, review times, recalls and adverse event reports over 20 years. 2007, this device’s year, is highlighted.
FDA decisions per year · FCX
1in 2024
2026 to Oct 25, outlined.
Median 510(k) review, days · FCX
Too few FCX 510(k)s in any year since 2007 to give a median.
Recalls per year · FCX
1in 2013
Class I (1 since 2007) Class II/III not classified
Adverse event reports per year · FCX
143in 2025
MAUDE reports naming product code FCX, 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 | 1 | — | 0 | 5 |
| 2008 | 0 | — | 0 | 11 |
| 2009 | 1 | — | 0 | 8 |
| 2010 | 0 | — | 0 | 20 |
| 2011 | 1 | — | 0 | 14 |
| 2012 | 1 | — | 0 | 13 |
| 2013 | 1 | — | 1 (1) | 19 |
| 2014 | 2 | — | 0 | 10 |
| 2015 | 0 | — | 0 | 5 |
| 2016 | 1 | — | 0 | 4 |
| 2017 | 0 | — | 0 | 3 |
| 2018 | 1 | — | 0 | 7 |
| 2019 | 1 | — | 0 | 4 |
| 2020 | 1 | — | 0 | 1 |
| 2021 | 1 | — | 0 | 12 |
| 2022 | 0 | — | 0 | 29 |
| 2023 | 1 | — | 0 | 54 |
| 2024 | 1 | — | 0 | 35 |
| 2025 | 0 | — | 0 | 143 |
| 2026 | 1 | — | 0 | — |
What is it indicated for?
This instrument has been designed to be used with Olympus gastrointestinal endoscopes and other ancillary equipment for CO 2 gas and water feeding.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K063786 · printed Nov 6, 2026
Cite this page
510(k) Report. “K063786: Endoscopic Insufflation Unit, Model Xecr-2.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K063786
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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