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

Alinity m EBV (09N43-095)

K Number: K243489 · Decision Jul 28, 2025
Classifications
1
FEI Numbers
7
Registration Numbers
7
Same Product Code
3
Applicant Total
17
Review Days
258

Basic Information

Device Name
Alinity m EBV (09N43-095)
K Number
K243489
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3183
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Abbott Molecular, Inc.
Date Received
November 12, 2024
Decision Date
July 28, 2025
Product Code
QLX
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
QLX Nucleic Acid Amplification Test For The Quantitation Of Epstein-Barr Virus (Ebv) Dna

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Other Clearances by Abbott Molecular, Inc.

K Number Device Name
K252102 Alinity m HCV
K243485 Alinity m CMV
K241921 Alinity m BKV
K241573 Alinity m Resp-4-Plex
K233349 Alinity m HSV 1 & 2 / VZV
K222379 Alinity m STI Assay
K212778 Alinity m EBV AMP Kit (List No. 09N43-095), Alinity m EBV CTRL Kit (List No. 09N43-085), Alinity m EBV CAL Kit (List No. 09N43-075)
K202977 Alinity m STI Assay
K140354 ABBOTT MULTI-COLLECT SPECIMEN COLLECTION KIT, ABBOTT REAL TIME CT/NG
K131508 VYSIS D7S486/CEP 7 FISH PROBE KIT
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