510(k) · Cleared
ClearedDimesol Tubing Sets for Hemodialysis
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Dimesol, Inc. · FJK Set, Tubing, Blood, With And Without Anti-Regurgitation Valve
Cleared on Mar 30, 2018 as substantially equivalent to K072024 (Nipro Medical Corp., 2007) and 1 other predicate after a 274-day review. Its family tree reaches back 2 generations to 1985.
- Decided
- Mar 30, 2018
- Review
- 274 days
- Class
- Class II
- Product code
- FJK
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 2 generations to K852605 (1985). 7 ancestors in all. No later device cites it as a predicate yet.
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −2 | K852605 | Blood Tubing Set | Medflex International, Inc. | 1985 | — |
| −1 | K032975 | JMS Blood Tubing Sets | Jms North America Corp. | 2004 | — |
| 0 (this device) | K171952 | Dimesol Tubing Sets for Hemodialysis | Dimesol, Inc. | 2018 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1996 | 1 | 0 |
| 2000 | 1 | 0 |
| 2001 | 2 | 0 |
| 2007 | 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 FJK? 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 FJK device
- #1 K252423 NovaLine Tubing Set for Hemodialysis (BL 124)score 12.2 · 4 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 |
|---|---|---|---|
| * | K072024 | Nipro Blood Tubing Set with Transducer Protector and Priming Set, Model A201-A219…Summary page 5…2-REVISED 510(K) SUMMARY UNDER 21 CFR 807.92 C. Legally Marketed Predicate Device(s) - Nipro Blood Tubing Set with Transducer Protector and Priming Set (K072024) - JMS Blood Tubing Sets (K032975) D. Device Description [0001] The Dimesol blood tubing sets for hemod… | 2007 |
| * | K032975 | JMS Blood Tubing SetsSummary page 5…2 C. Legally Marketed Predicate Device(s) - Nipro Blood Tubing Set with Transducer Protector and Priming Set (K072024) - JMS Blood Tubing Sets (K032975) D. Device Description [0001] The Dimesol blood tubing sets for hemodialysis are single use arterial and venous… | 2004 |
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?
- The line of descent spans 33 years and passes through 3 companies; a new generation was cleared every 19.0 years on median.
- 1 of the 7 ancestors has a recall of any class.
- 5 other devices also cite its predicate K072024.
How does its category compare?
All FJK devicesFJK Set, Tubing, Blood, With And Without Anti-Regurgitation Valve: FDA decisions, review times, recalls and adverse event reports over 20 years. 2018, this device’s year, is highlighted.
FDA decisions per year · FJK
1in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · FJK
255in 2021
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · FJK
1in 2025
Class I (1 since 2007) Class II/III not classified
Adverse event reports per year · FJK
1,487in 2025
MAUDE reports naming product code FJK, 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 | 4 | 116 | 2 | 135 |
| 2008 | 1 | — | 2 | 86 |
| 2009 | 1 | — | 0 | 76 |
| 2010 | 1 | — | 2 | 130 |
| 2011 | 0 | — | 0 | 243 |
| 2012 | 2 | — | 0 | 35 |
| 2013 | 0 | — | 0 | 114 |
| 2014 | 1 | — | 0 | 116 |
| 2015 | 0 | — | 1 | 126 |
| 2016 | 1 | — | 0 | 139 |
| 2017 | 1 | — | 0 | 131 |
| 2018 | 1 | — | 0 | 119 |
| 2019 | 0 | — | 0 | 185 |
| 2020 | 0 | — | 1 | 190 |
| 2021 | 3 | 255 | 0 | 188 |
| 2022 | 0 | — | 0 | 362 |
| 2023 | 1 | — | 0 | 585 |
| 2024 | 1 | — | 0 | 417 |
| 2025 | 1 | — | 1 (1) | 1,487 |
| 2026 | 2 | — | 1 | — |
What is it indicated for?
The Dimesol Tubing Sets for Hemodialysis are single-use sterile medical devices intended to
connect the patient to the hemodialyzer and the hemodialysis delivery system in hemodialysis
treatment. The compatibility of available configurations is the responsibility of the physician /
clinician in charge.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K171952 · printed Nov 6, 2026
Cite this page
510(k) Report. “K171952: Dimesol Tubing Sets for Hemodialysis.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K171952
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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