Access anti-HAV IgM
FDA 510(k) K251995 · Beckman Coulter, Inc.
510(k) numberK251995
Submission
- Device name
- Access anti-HAV IgM
- Applicant
- Beckman Coulter, Inc.
Chaska, MN, US - Received
- June 27, 2025
- Decision date
- January 27, 2026
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- LOL – Hepatitis A Test (Antibody And Igm Antibody)
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 866.3310
- Specialty
- Microbiology
Other 510(k)s with product code LOL
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K260048 | Elecsys Anti-HAV IgMLOL · Traditional | Roche Diagnostics | 04/07/2026SE |
| K243846 | Access anti-HAVLOL · Traditional | Beckman Coulter, Inc. | 09/09/2025SE |
| K222850 | HAVAb IgG IILOL · Traditional | Abbott Laboratories | 08/10/2023SE |
| K223403 | LIAISON Anti-HAV; LIAISON XSLOL · Special | DiaSorin, Inc. | 12/09/2022SE |
| K210272 | LIAISON Anti-HAVLOL · Special | DiaSorin, Inc. | 02/09/2021SE |
| K193532 | LIAISON Anti-HAV AssayLOL · Traditional | DiaSorin, Inc. | 03/02/2020SE |
| K190428 | Elecsys Anti-HAV IILOL · Traditional | Roche Diagnostics | 08/13/2019SE |
| K161964 | ADVIA Centaur HAV IgM AssayLOL · Traditional | Siemens Healthcare Diagnostics, Inc. | 10/13/2016SE |
| K160650 | LIAISON HAV IgM, LIAISON Control HAV IgMLOL · Traditional | DiaSorin, Inc. | 08/25/2016SE |
| K142758 | ADVIA Centaur HAV total assayLOL · Traditional | Siemens Healthcare Diagnostics, Inc. | 12/05/2014SE |
More from Siemens Healthcare Diagnostics, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K252169 | Access BNP IINBC · Traditional | 03/24/2026SE |
| K254059 | Access anti-HBc IgMSEI · Traditional | 03/13/2026SE |
| K253687 | Access anti-HBc TotalSEI · Traditional | 02/19/2026SE |
| K250588 | Access Rubella IgGLFX · Traditional | 11/17/2025SE |
| K252580 | iQ200 SeriesLKM · Special | 09/10/2025SE |
| K243846 | Access anti-HAVLOL · Traditional | 09/09/2025SE |
| K243804 | MicroScan Dried Gram-Negative MIC/Combo Panels with Cefepime (CPE) (0.12-64 µg/mL)…LTT · Traditional | 08/20/2025SE |
| K250036 | MicroScan Dried Gram-Positive MIC/Combo Panels with Daptomycin (DAP) (0.06-32 µg/mL)LTT · Traditional | 08/15/2025SE |
| K243483 | Access hsTnIMMI · Traditional | 08/01/2025SE |
| K250084 | MicroScan Dried Gram-Negative MIC/Combo Panels with Aztreonam (AZT) (0.5-64 µg/mL)LTT · Traditional | 07/18/2025SE |
Questions and answers
When was Access anti-HAV IgM cleared by the FDA?
Access anti-HAV IgM (K251995) received a 510(k) decision of Substantially Equivalent on January 27, 2026, 214 days after the submission was received.
What is the product code of K251995?
The FDA product code is LOL – Hepatitis A Test (Antibody And Igm Antibody), a Class II (moderate risk) device regulated under 21 CFR 866.3310.