510(k) K243168
- Device
- Alinity i Rubella IgG
- Applicant
- Abbott Laboratories
- 510(k) number
- K243168
- Product code
- LFX
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 2025-06-20
- Date received
- 2024-09-30
- Regulation
- 866.3510
- Classification name
- Enzyme Linked Immunoabsorbent Assay, Rubella
- Medical specialty
- Microbiology
- Review panel
- Microbiology
- Device class
- 2
- Clearance type
- Traditional
- Statement or summary
- Summary
- Third party reviewed
- N
- Source
- FDA openFDA 510(k) dataset plus migrated FDA.report data
Related Records
Applicant Contact
- Contact
- Laura Fraczek
- Address
- 100 Abbott Park Rd. Abbott Park IL US 60064 60064
FDA Registration Numbers
- 9610126
- 1219913
- 3002809144
- 1318354
- 2020726
- 3022178699
- 2122870
- 8020888
- 2432235
- 3005529799
- 3032705
- 1036362
- 9610240
- 2246703
- 2029372
- 3002806944
- 9615037
- 8031673
- 3007208259
- 3005333358
- 2242436
- 3007111389
- 3033967997
- 1827821
- 3003030793
- 8023060
- 9612316
- 1641328
- 8020790
- 1928237
- 1319681
- 3008344661
- 3006198300
Source Documents
FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON
Other 510(k) Records For Product Code LFX
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K250588 | Access Rubella IgG | Beckman Coulter, Inc. | 2025-11-17 |
| K122397 | LIAISON RUBELLA IGM, LIAISON CONTROL RUBELLA IGM | DiaSorin, Inc. | 2012-09-06 |
| K093101 | MAGO 4S | Diamedix Corp. | 2011-01-21 |
| K092587 | BIOPLEX 2200 RUBELLA & CMV IGM KIT ON THE BIOPLEX 2200 MULTI ANALYTE DETECTION SYSTEM | Bio-Rad Laboratories | 2010-12-03 |
| K092322 | ELECSYS RUBELLA IGM IMMUNOASSAY | Roche Diagnostics | 2010-03-12 |
| K080766 | VIDAS RUB IGG | bioMerieux, Inc. | 2008-12-23 |
| K072617 | ELECSYS RUBELLA IGG IMMUNOASSAY | Roche Diagnostics Corp. | 2008-12-05 |
| K073390 | DIASORIN LIASON RUBELLA IGG ASSAY; DIASORIN LIAISON RUBELLA IGG TRI-CONTROLS | DiaSorin, Inc. | 2008-11-21 |
| K063186 | ATHENA MULTI-LYTE RUBELLA IGG TEST SYSTEM | Zeus Scientific, Inc. | 2007-03-21 |
| K063143 | VITROS IMMUNODIAGNOSTIC PRODUCTS RUBELLA IGG REAGANT PACK AND CALIBRATORS | Ortho-Clinical Diagnostics, Inc. | 2006-12-26 |
| K031606 | ACCESS IMMUNOASSAY SYSTEM RUBELLA IGG ASSAY | Beckman Coulter, Inc. | 2003-06-20 |
| K012077 | IMMULITE RUBELLA IGM,LKRM1, LKRM2, IMMULITE 2000 RUBELLA IGM, MODEL L2KRM2, L2KRM6 | Diagnostic Products Corp. | 2002-01-10 |
| K010668 | BAYER DIAGNOSTICS ADVIA CENTAUR RUBELLA IGM ASSAY | Bayer Corp. | 2001-07-05 |
| K003412 | ADVIA CENTAUR RUBELLA IGG ASSAY | Bayer Corp. | 2001-04-13 |
| K001875 | DIAMEDIX IS-RUBELLA IGM CAPTURE TEST SYSTEM | Diamedix Corp. | 2000-08-21 |