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

Access Rubella IgG

K Number: K250588 · Decision Nov 17, 2025
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
93
Applicant Total
270
Review Days
263

Basic Information

Device Name
Access Rubella IgG
K Number
K250588
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3510
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Beckman Coulter, Inc.
Date Received
February 27, 2025
Decision Date
November 17, 2025
Product Code
LFX
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
LFX Enzyme Linked Immunoabsorbent Assay, Rubella

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