510(k) · Cleared
Recalled · Class II · 2018Vitros Immunodiagnostic Products Vitamin B12, Reagent Pack 1/2, Folate Reagent Pack 3, Calibrators
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Ortho-Clinical Diagnostics · CDD Radioassay, Vitamin B12
Cleared on Jan 24, 2002 as substantially equivalent to K933142 (Bio-Rad Laboratories, Inc., 1993) after a 62-day review. Its family tree reaches back 1 generation to 1993. It has been recalled 2 times.
- Decided
- Jan 24, 2002
- Review
- 62 days
- Class
- Class II
- Product code
- CDD
- Recalls
- 2
- Predicates
- 1
Its longest line of descent runs back 1 generation to K933142 (1993). No later device cites it as a predicate yet.
- Root · 1 generation backK933142 Access Vitamin B12 AssayBio-Rad Laboratories, Inc. · 1993
- This deviceK013899 Vitros Immunodiagnostic Products Vitamin B12, Reagent Pack 1/2…Ortho-Clinical Diagnostics · 2002
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K933142 | Access Vitamin B12 Assay | Bio-Rad Laboratories, Inc. | 1993 | — |
| 0 (this device) | K013899 | Vitros Immunodiagnostic Products Vitamin B12, Reagent Pack 1/2, Folate Reagent… | Ortho-Clinical Diagnostics | 2002 | — |
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 CDD? 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 CDD device
- #1 K233541 ARCHITECT Active-B12 (Holotranscobalamin)score 8.7 · 4 generations · no Class I recall
- #2 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 |
|---|---|---|---|
| * | K933142 | Access Vitamin B12 AssaySummary page 1…ion Name: Vitamin B12 test system (862.1810) The VITROS Immunodiagnostic Products Vitamin B12 Assay is substantially equivalent to the BECKMAN Access Vitamin B12 assay (K933142). Continued on next page Ortho-Clinical Diagnosfics VITROS Immunodiagnostic Products Vitamin B12 Assay 1 510(k)… | 1993 |
What descends from it?
No later submission names this one as a predicate yet.
Has anything in its family been recalled? (0 Class I)
Recalls of this device
| Date | Class | Recall | Root cause | Reason |
|---|---|---|---|---|
| Aug 28, 2018 | Class II | Z-0392-2019 | Under Investigation by firm | The reagent pack exhibits the potential for an increased frequency of calibration failures. |
| Dec 18, 2002 | Not classified | Z-0557-03 | Other | Cartons labeled 'TDM Performance Verifier I' may contain TDM Performance Verified II. |
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 CDD devicesCDD Radioassay, Vitamin B12: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · CDD
1in 2024
2026 to Oct 25, outlined.
Median 510(k) review, days · CDD
147in 2012
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · CDD
1in 2021
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · CDD
44in 2025
MAUDE reports naming product code CDD, 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 | 1 | — | 1 | 0 |
| 2008 | 0 | — | 0 | 0 |
| 2009 | 1 | — | 0 | 0 |
| 2010 | 1 | — | 0 | 4 |
| 2011 | 3 | 117 | 0 | 36 |
| 2012 | 3 | 147 | 0 | 23 |
| 2013 | 1 | — | 0 | 45 |
| 2014 | 2 | — | 0 | 12 |
| 2015 | 1 | — | 0 | 4 |
| 2016 | 2 | — | 0 | 6 |
| 2017 | 1 | — | 0 | 9 |
| 2018 | 0 | — | 2 | 15 |
| 2019 | 2 | — | 1 | 14 |
| 2020 | 0 | — | 0 | 11 |
| 2021 | 0 | — | 1 | 28 |
| 2022 | 1 | — | 0 | 24 |
| 2023 | 0 | — | 0 | 27 |
| 2024 | 1 | — | 0 | 33 |
| 2025 | 0 | — | 0 | 44 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The VITROS Immunodiagnostic Products Vitamin B12 Reagent Pack 1/ 2 and the VITROS Immunodiagnostic Products Vitamin B12/ Folate Reagent Pack 3 quantitatively measures vitamin B12 concentration in human serum and plasma (EDTA or heparin), to aid in the diagnosis of anemia using the VITROS ECi Immunodiagnostic System with Intellicheck.
The VITROS Immunodiagnostic Products Vitamin B12 Calibrators- for use in the calibration of the Vitros Immunodiagnostic System for the quantitative measurement of vitamin B12 in human serum and plasma (EDTA or heparin).
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/K013899 · printed Nov 4, 2026
Cite this page
510(k) Report. “K013899: Vitros Immunodiagnostic Products Vitamin B12, Reagent Pack 1/2, Folate Reagent Pack 3, Calibrators.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K013899
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 30, 2026 (extraction version 2d9447fa9ea4)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026