510(k) · Cleared
ClearedModification to Liquichek Spinal Fluid Control, Item Nos. 751, 752
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Bio-Rad · JJY Multi-Analyte Controls, All Kinds (Assayed)
Cleared on Apr 7, 1999 as substantially equivalent to K932076 (Bio-Rad, 1993) after a 28-day review. Its family tree reaches back 1 generation to 1993. 1 later device descends from it.
- Decided
- Apr 7, 1999
- Review
- 28 days
- Class
- Class I
- Product code
- JJY
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 1 generation to K932076 (1993). 1 later device descends from it, 1 citing it directly.
- Root · 1 generation backK932076 Liquichek Spinal Fluid Control Levels I and IIBio-Rad · 1993
- This deviceK990888 Modification to Liquichek Spinal Fluid Control, Item Nos. 751, 752Bio-Rad · 1999
- Descendant · cites it directly · 0 of its ownK123775 Liquichek Spinal Fluid Control Level 1, Liquichek Spinal Fluid…Bio-Rad Laboratories · 2013
Most influential descendants
Showing 1 of 1 · See all- K123775Liquichek Spinal Fluid Control Level 1, Liquichek Spinal Fluid Control Level 2…Bio-Rad Laboratories · 2013 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K932076 | Liquichek Spinal Fluid Control Levels I and II | Bio-Rad | 1993 | — |
| 0 (this device) | K990888 | Modification to Liquichek Spinal Fluid Control, Item Nos. 751, 752 | Bio-Rad | 1999 | — |
| +1 | K123775 | Liquichek Spinal Fluid Control Level 1, Liquichek Spinal Fluid Control Level… | Bio-Rad Laboratories | 2013 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2013 | 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 JJY? 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 |
|---|---|---|---|
| * | K932076 | Liquichek Spinal Fluid Control Levels I and IISummary page 1…Control, All Kinds (Assayed and Unassayed) Devices to Which Substantial Equivalence is Claimed Liquichek Spinal Fluid Control Bio-Rad Laboratories Irvine, California K932076 Statement of Intended Use Liquichek Spinal Fluid Control is intended for use as an assayed quality control to monitor the preci… | 1993 |
What descends from it? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K123775 | Liquichek Spinal Fluid Control Level 1, Liquichek Spinal Fluid Control Level 2… | 2013 | 0 |
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.
- Of its descendants, K123775 (Bio-Rad Laboratories, 2013) has gone furthest, with 0 descendants of its own.
How does its category compare?
All JJY devicesJJY Multi-Analyte Controls, All Kinds (Assayed): FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · JJY
3in 2017
2026 to Oct 25, outlined.
Median 510(k) review, days · JJY
78in 2017
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · JJY
2in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · JJY
13in 2025
MAUDE reports naming product code JJY, 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 | 11 | 49 | 5 | 2 |
| 2008 | 7 | 54 | 0 | 1 |
| 2009 | 8 | 80 | 2 | 3 |
| 2010 | 10 | 109 | 6 | 3 |
| 2011 | 14 | 120 | 1 | 6 |
| 2012 | 13 | 40 | 3 | 20 |
| 2013 | 16 | 82 | 2 | 5 |
| 2014 | 10 | 49 | 2 | 4 |
| 2015 | 4 | 153 | 1 | 4 |
| 2016 | 1 | — | 3 | 13 |
| 2017 | 3 | 78 | 4 | 12 |
| 2018 | 0 | — | 3 | 7 |
| 2019 | 0 | — | 4 | 1 |
| 2020 | 0 | — | 6 | 7 |
| 2021 | 0 | — | 0 | 1 |
| 2022 | 0 | — | 3 | 0 |
| 2023 | 0 | — | 3 | 4 |
| 2024 | 0 | — | 0 | 1 |
| 2025 | 0 | — | 2 | 13 |
| 2026 | 0 | — | 1 | — |
What is it indicated for?
Liquichek Spinal Fluid Control is intended for use as an assayed quality control to monitor the precision of laboratory testing procedures for the analytes listed in the package insert.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K990888 · printed Nov 6, 2026
Cite this page
510(k) Report. “K990888: Modification to Liquichek Spinal Fluid Control, Item Nos. 751, 752.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K990888
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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