FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Access anti-HAV IgM

K Number: K251995 · Decision Jan 27, 2026
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
25
Applicant Total
270
Review Days
214

Basic Information

Device Name
Access anti-HAV IgM
K Number
K251995
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3310
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Beckman Coulter, Inc.
Date Received
June 27, 2025
Decision Date
January 27, 2026
Product Code
LOL
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LOL Hepatitis A Test (Antibody And Igm Antibody)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LOL), ordered by most recent decision date.

View all

Other Clearances by Beckman Coulter, Inc.

K Number Device Name
K252169 Access BNP II
K254059 Access anti-HBc IgM
K253687 Access anti-HBc Total
K250588 Access Rubella IgG
K252580 iQ200 Series
K243846 Access anti-HAV
K243804 MicroScan Dried Gram-Negative MIC/Combo Panels with Cefepime (CPE) (0.12-64 µg/mL) (MicroScan)
K250036 MicroScan Dried Gram-Positive MIC/Combo Panels with Daptomycin (DAP) (0.06-32 µg/mL)
K243483 Access hsTnI
K250084 MicroScan Dried Gram-Negative MIC/Combo Panels with Aztreonam (AZT) (0.5-64 µg/mL)
Search all 270 clearances from Beckman Coulter, Inc. →