510(k) · Cleared
Cleared14Fr Colon Decompression Set, Macon Colon Decompression Set
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Cook Ireland, Ltd. · FEG Tube, Double Lumen For Intestinal Decompression And/Or Intubation
Cleared on Aug 1, 2017 as substantially equivalent to K900035 (Wilson-Cook Medical, Inc., 1990) after a 60-day review. Its family tree reaches back 1 generation to 1990.
- Decided
- Aug 1, 2017
- Review
- 60 days
- Class
- Class II
- Product code
- FEG
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 1 generation to K900035 (1990). No later device cites it as a predicate yet.
- Root · 1 generation backK900035 Wilson-Cook Colon Decompression SetWilson-Cook Medical, Inc. · 1990 · Recalled
- This deviceK171619 14Fr Colon Decompression Set, Macon Colon Decompression SetCook Ireland, Ltd. · 2017
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K900035 | Wilson-Cook Colon Decompression Set | Wilson-Cook Medical, Inc. | 1990 | 2 |
| 0 (this device) | K171619 | 14Fr Colon Decompression Set, Macon Colon Decompression Set | Cook Ireland, Ltd. | 2017 | — |
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 FEG? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
- Candidate predicates for a device like this, rankedin the report
- Recall history across each candidate’s familyin the 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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K900035 | Wilson-Cook Colon Decompression SetSummary page 5…Cook 14Fr and Marcon Colon Decompression Set Page 2 of 4 III. PREDICATE DEVICE Predicate: Cook Colon Decompression Set, K900035 cleared on March 07, 1990. IV. DEVICE DESCRIPTION 14Fr Colon Decompression Set (CDSG) The CDSG device consists of a colon deco… | 1990 |
What descends from it?
No later submission names this one as a predicate yet.
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?
- Its one ancestor has a recall.
How does its category compare?
All FEG devicesFEG Tube, Double Lumen For Intestinal Decompression And/Or Intubation: FDA decisions, review times, recalls and adverse event reports over 20 years. 2017, this device’s year, is highlighted.
FDA decisions per year · FEG
1in 2017
2026 to Oct 25, outlined.
Median 510(k) review, days · FEG
Too few FEG 510(k)s in any year since 2007 to give a median.
Recalls per year · FEG
2in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · FEG
46in 2025
MAUDE reports naming product code FEG, 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 | 1 |
| 2009 | 0 | — | 0 | 3 |
| 2010 | 0 | — | 0 | 1 |
| 2011 | 0 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 2 |
| 2013 | 1 | — | 0 | 2 |
| 2014 | 0 | — | 0 | 5 |
| 2015 | 0 | — | 0 | 1 |
| 2016 | 0 | — | 0 | 4 |
| 2017 | 1 | — | 0 | 13 |
| 2018 | 0 | — | 0 | 15 |
| 2019 | 0 | — | 0 | 36 |
| 2020 | 0 | — | 0 | 23 |
| 2021 | 0 | — | 0 | 27 |
| 2022 | 0 | — | 0 | 40 |
| 2023 | 0 | — | 10 | 33 |
| 2024 | 0 | — | 0 | 31 |
| 2025 | 0 | — | 2 | 46 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
This device is used for treatment of acute non-toxic megacolon, pseudo-obstruction (Ogilvie’s syndrome) and colonic strictures.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K171619 · printed Nov 6, 2026
Cite this page
510(k) Report. “K171619: 14Fr Colon Decompression Set, Macon Colon Decompression Set.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K171619
Report an extraction error
Are you the manufacturer?
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