510(k) · Cleared
ClearedSerim Hisense Ultra 0.1, Part Number 5167
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Serim Research Corp. · MSY Strip, Test, Reagent, Residuals For Dialysate, Disinfectant
Cleared on May 6, 2008 as substantially equivalent to K001194 (Environmental Test Systems, Inc., 2000) after a 54-day review. Its family tree reaches back 1 generation to 2000.
- Decided
- May 6, 2008
- Review
- 54 days
- Class
- Class II
- Product code
- MSY
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 1 generation to K001194 (2000). No later device cites it as a predicate yet.
- Root · 1 generation backK001194 Sterichek Total Chlorine Reagent StripsEnvironmental Test Systems, Inc. · 2000
- This deviceK080712 Serim Hisense Ultra 0.1, Part Number 5167Serim Research Corp. · 2008
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K001194 | Sterichek Total Chlorine Reagent Strips | Environmental Test Systems, Inc. | 2000 | — |
| 0 (this device) | K080712 | Serim Hisense Ultra 0.1, Part Number 5167 | Serim Research Corp. | 2008 | — |
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 MSY? 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 MSY device
- #1 K243898 Chlorine Sentinel IIscore 9.5 · 2 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin 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 |
|---|---|---|---|
| * | K001194 | Sterichek Total Chlorine Reagent Strips | 2000 |
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 no recall.
How does its category compare?
All MSY devicesMSY Strip, Test, Reagent, Residuals For Dialysate, Disinfectant: FDA decisions, review times, recalls and adverse event reports over 20 years. 2008, this device’s year, is highlighted.
FDA decisions per year · MSY
1in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · MSY
Too few MSY 510(k)s in any year since 2007 to give a median.
Recalls per year · MSY
No recall names MSY since 2007.
Adverse event reports per year · MSY
1in 2011
MAUDE reports naming product code MSY, 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 | 2 |
| 2008 | 1 | — | 0 | 35 |
| 2009 | 1 | — | 0 | 0 |
| 2010 | 0 | — | 0 | 0 |
| 2011 | 0 | — | 0 | 1 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 0 | — | 0 | 0 |
| 2014 | 1 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 0 | — | 0 | 0 |
| 2017 | 0 | — | 0 | 0 |
| 2018 | 0 | — | 0 | 0 |
| 2019 | 0 | — | 0 | 0 |
| 2020 | 1 | — | 0 | 0 |
| 2021 | 0 | — | 0 | 0 |
| 2022 | 1 | — | 0 | 0 |
| 2023 | 0 | — | 0 | 0 |
| 2024 | 0 | — | 0 | 0 |
| 2025 | 1 | — | 0 | 0 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
SERIM® HiSENSE ULTRA 0.1TM Test Strips provide a convenient means for indicating the concentration of residual chlorine (chlorine bleach) detected in the solution used to rinse dialysate lines following disinfection of hemodialysis equipment. HiSENSE ULTRA 0.1 also provides a quick and convenient means for indicating low levels of total chlorine (chloramines/free chlorine) in water used to prepare dialysate.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K080712 · printed Nov 3, 2026
Cite this page
510(k) Report. “K080712: Serim Hisense Ultra 0.1, Part Number 5167.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K080712
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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