510(k) K233349

Device
Alinity m HSV 1 & 2 / VZV
Applicant
Abbott Molecular, Inc.
510(k) number
K233349
Product code
PGI
Decision
Substantially Equivalent (SESE)
Decision date
2024-05-03
Date received
2023-09-29
Regulation
866.3309
Classification name
Herpes Virus (Vzv, Hsv1, Hsv2), Dna Detection Assay For Cutaneous And Mucocutaneous Lesion Samples
Medical specialty
Microbiology
Review panel
Microbiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Stacy Ferguson
Address
1300 E Touhy Ave. Des Plaines IL US 60018 60018

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code PGI#

510(k), Device, Applicant table
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K173798Simplexa HSV 1 & 2 Direct, Simplexa HSV 1 & 2 Positive Control PackDiasorin Molecular, LLC2018-03-14
K162451Solana HSV 1+2/VZV AssayQuidel Corporation2016-11-28
K151906ARIES HSV 1&2 Assay Cassettes - Carton of 24 (IVD), ARIES HSV 1&2 Assay Protocol File Kit (IVD), ARIES HSV 1&2 Assay Cassette (IVD)Luminex Corporation2015-10-06
K151046illumigene HSV 1&2 DNA Amplification Assay, illumigene HSV 1&2 External Control Kit, illumipro-10Meridian Bioscience, Inc.2015-07-17
DEN140004QUIDEL MOLECULAR DIRECT HSV 1 +2/VZV ASSAYDiagnostic Hybrids, Inc.2014-05-13