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

Access anti-HAV

K Number: K243846 · Decision Sep 9, 2025
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
25
Applicant Total
270
Review Days
267

Basic Information

Device Name
Access anti-HAV
K Number
K243846
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
December 16, 2024
Decision Date
September 9, 2025
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)

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K Number Device Name
K252169 Access BNP II
K254059 Access anti-HBc IgM
K253687 Access anti-HBc Total
K251995 Access anti-HAV IgM
K250588 Access Rubella IgG
K252580 iQ200 Series
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)
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