510(k) · Cleared
ClearedCiba Corning 288 PH/Blood Gas System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Ciba Corning Diagnostics Corp. · JQY Ph Meter
Cleared on Aug 25, 1987 after a 33-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 8 later devices descend from it.
- Decided
- Aug 25, 1987
- Review
- 33 days
- Class
- Class I
- Product code
- JQY
- Recalls
- None
- Predicates
- 0
8 later devices descend from it, 1 citing it directly.
- This deviceK872888 Ciba Corning 288 PH/Blood Gas SystemCiba Corning Diagnostics Corp. · 1987
- Descendant · cites it directly · 7 of its ownK050423 Omni Modular, Omni C and Omni S Analyzer (PH Electrode)Roche Diagnostics · 2005
- Descendant · 2 generations on · 5 of its ownK110416 ABL835 Flex Analyzer with Pleural PHRadiometer Medical Aps · 2011 · Recalled
- Descendant · 3 generations on · 4 of its ownK122539 Measurement of PH in Pleural Fluid on Blood Gas SystemSiemens Healthcare Diagnostics · 2013
- Descendant · 4 generations on · 3 of its ownK192240 RAPIDPoint 500e Blood Gas SystemSiemens Healthcare Diagnostics, Inc. · 2020 · Recalled
- Descendant · 5 generations on · 1 of its ownK223857 i-STAT G3+ cartridge with the i-STAT 1 SystemAbbott Point of Care, Inc. · 2023 · Recalled
Showing 5 of 8 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 8 · See all- K050423Omni Modular, Omni C and Omni S Analyzer (PH Electrode)Roche Diagnostics · 2005 · cites it directly7descendants
- K110416ABL835 Flex Analyzer with Pleural PHRadiometer Medical Aps · 2011 · 2 generations on5descendants
- K122539Measurement of PH in Pleural Fluid on Blood Gas SystemSiemens Healthcare Diagnostics · 2013 · 3 generations on4descendants
- K192240RAPIDPoint 500e Blood Gas SystemSiemens Healthcare Diagnostics, Inc. · 2020 · 4 generations on3descendants
- K223857i-STAT G3+ cartridge with the i-STAT 1 SystemAbbott Point of Care, Inc. · 2023 · 5 generations on1descendant
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K872888 | Ciba Corning 288 PH/Blood Gas System | Ciba Corning Diagnostics Corp. | 1987 | — |
| +1 | K050423 | Omni Modular, Omni C and Omni S Analyzer (PH Electrode) | Roche Diagnostics | 2005 | — |
| +2 | K110416 | ABL835 Flex Analyzer with Pleural PH | Radiometer Medical Aps | 2011 | 2 |
| +3 | K122539 | Measurement of PH in Pleural Fluid on Blood Gas System | Siemens Healthcare Diagnostics | 2013 | — |
| +4 | K192240 | RAPIDPoint 500e Blood Gas System | Siemens Healthcare Diagnostics, Inc. | 2020 | 4 |
| +5 | K223857 | i-STAT G3+ cartridge with the i-STAT 1 System | Abbott Point of Care, Inc. | 2023 | 1 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2005 | 1 | 0 |
| 2010 | 1 | 0 |
| 2011 | 1 | 0 |
| 2013 | 1 | 0 |
| 2020 | 1 | 0 |
| 2023 | 2 | 0 |
| 2025 | 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 JQY? 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?
FDA has not posted a summary or statement for it, so its predicates are not known.
What descends from it? (8)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K050423 | Omni Modular, Omni C and Omni S Analyzer (PH Electrode) | 2005 | 7 |
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?
- Of its descendants, K050423 (Roche Diagnostics, 2005) has gone furthest, with 7 descendants of its own.
How does its category compare?
All JQY devicesJQY Ph Meter: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · JQY
FDA has decided no JQY device since 2007.
Median 510(k) review, days · JQY
Too few JQY 510(k)s in any year since 2007 to give a median.
Recalls per year · JQY
No recall names JQY since 2007.
Adverse event reports per year · JQY
No MAUDE report names JQY since 2007.
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 | 0 |
| 2009 | 0 | — | 0 | 0 |
| 2010 | 0 | — | 0 | 0 |
| 2011 | 0 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 0 | — | 0 | 0 |
| 2014 | 0 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 0 | — | 0 | 0 |
| 2017 | 0 | — | 0 | 0 |
| 2018 | 0 | — | 0 | 0 |
| 2019 | 0 | — | 0 | 0 |
| 2020 | 0 | — | 0 | 0 |
| 2021 | 0 | — | 0 | 0 |
| 2022 | 0 | — | 0 | 0 |
| 2023 | 0 | — | 0 | 0 |
| 2024 | 0 | — | 0 | 0 |
| 2025 | 0 | — | 0 | 0 |
| 2026 | 0 | — | 0 | — |
https://510kreport.com/device/K872888 · printed Nov 5, 2026
Cite this page
510(k) Report. “K872888: Ciba Corning 288 PH/Blood Gas System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K872888
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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