510(k) · Cleared
Recalled · 2012Microstream Oral Nasal Cannula Filterline
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Oridion Medical 1987, Ltd. · CCK Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase
Cleared on May 4, 2001 after a 28-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 3 later devices descend from it. It has been recalled 3 times.
- Decided
- May 4, 2001
- Review
- 28 days
- Class
- Class II
- Product code
- CCK
- Recalls
- 3
- Predicates
- 0
3 later devices descend from it, 3 citing it directly.
- This deviceK011050 Microstream Oral Nasal Cannula FilterlineOridion Medical 1987, Ltd. · 2001
- Descendant · cites it directly · 0 of its ownK173147 SuperNO2VA Et DeviceRevolutionary Medical Devices, Inc. · 2018
- Descendant · cites it directly · 0 of its ownK143127 CO2-Mas, Oxygen Delivery/ CO2 sampling cannula style, CO2 sampling…Dispo-Med (Malaysia) Sdn Bhd · 2015
- Descendant · cites it directly · 0 of its ownK012394 Oridion Mac-Line Oral Nasal Cannula Sample LineOridion Medical 1987, Ltd. · 2001
Most influential descendants
Showing 3 of 3 · See all- K173147SuperNO2VA Et DeviceRevolutionary Medical Devices, Inc. · 2018 · cites it directly0descendants
- K143127CO2-Mas, Oxygen Delivery/ CO2 sampling cannula style, CO2 sampling only styleDispo-Med (Malaysia) Sdn Bhd · 2015 · cites it directly0descendants
- K012394Oridion Mac-Line Oral Nasal Cannula Sample LineOridion Medical 1987, Ltd. · 2001 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K011050 | Microstream Oral Nasal Cannula Filterline | Oridion Medical 1987, Ltd. | 2001 | — |
| +1 | K173147 | SuperNO2VA Et Device | Revolutionary Medical Devices, Inc. | 2018 | — |
| +1 | K143127 | CO2-Mas, Oxygen Delivery/ CO2 sampling cannula style, CO2 sampling only style | Dispo-Med (Malaysia) Sdn Bhd | 2015 | — |
| +1 | K012394 | Oridion Mac-Line Oral Nasal Cannula Sample Line | Oridion Medical 1987, Ltd. | 2001 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2001 | 1 | 0 |
| 2015 | 1 | 0 |
| 2018 | 1 | 0 |
Sources: FDA 510(k) database (decision fields), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in CCK? 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 CCK device
- #1 K253030 Capnostream™35 Portable Respiratory Monitor…score 15.8 · 16 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against?
FDA has not posted a summary or statement for it, so its predicates are not known.
What descends from it? (3)
3 later devices cite it directly; ranked here by how many devices descend from each in turn.
Has anything in its family been recalled? (0 Class I)
Recalls of this device
| Date | Class | Recall | Root cause | Reason |
|---|---|---|---|---|
| Feb 16, 2012 | Not classified | Z-1332-2012 | Packaging process control | CO2 sampling lines may have paper and plastic particulate present in the packaged units at levels that may exceed visual specification. |
| May 26, 2010 | Not classified | Z-2006-2010 | Process design | The Microstream Filterline may not be recognized by the monitor when connected. No CO2 readings will be displayed and no alarms may sound for unmonitored patients. Replacing the filterline may delay treatment. |
| May 26, 2010 | Not classified | Z-2003-2010 | Process design | The Microstream Filterline may not be recognized by the monitor when connected. No CO2 readings will be displayed and no alarms may sound for unmonitored patients. Replacing the filterline may delay treatment. |
No ancestor or descendant has a Class I recall.
What does this lineage say?
- Of its descendants, K173147 (Revolutionary Medical Devices, Inc., 2018) has gone furthest, with 0 descendants of its own.
How does its category compare?
All CCK devicesCCK Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · CCK
3in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · CCK
169in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · CCK
1in 2022
Class I (8 since 2007) Class II/III not classified
Adverse event reports per year · CCK
1,259in 2025
MAUDE reports naming product code CCK, 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 | 5 | 56 | 0 | 7 |
| 2008 | 3 | 248 | 1 | 20 |
| 2009 | 3 | 101 | 19 | 21 |
| 2010 | 3 | 125 | 4 | 12 |
| 2011 | 2 | — | 14 | 18 |
| 2012 | 7 | 150 | 3 | 13 |
| 2013 | 4 | 132 | 2 (1) | 28 |
| 2014 | 9 | 166 | 0 | 51 |
| 2015 | 5 | 105 | 1 | 114 |
| 2016 | 2 | — | 0 | 88 |
| 2017 | 5 | 134 | 0 | 58 |
| 2018 | 6 | 296 | 5 | 63 |
| 2019 | 7 | 261 | 7 (7) | 141 |
| 2020 | 4 | 188 | 1 | 2,302 |
| 2021 | 4 | 227 | 0 | 2,272 |
| 2022 | 3 | 226 | 1 | 2,475 |
| 2023 | 4 | 555 | 0 | 1,637 |
| 2024 | 3 | 592 | 0 | 1,216 |
| 2025 | 3 | 169 | 0 | 1,259 |
| 2026 | 3 | 224 | 0 | — |
https://510kreport.com/device/K011050 · printed Nov 4, 2026
Cite this page
510(k) Report. “K011050: Microstream Oral Nasal Cannula Filterline.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K011050
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Record history
- FDA decision record loaded May 2, 2026
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026