Elecsys HSV-2 IgG (08948887160)

FDA 510(k) K220924 · Roche Diagnostics

Substantially Equivalent

510(k) numberK220924

Submission

Device name
Elecsys HSV-2 IgG (08948887160)
Applicant
Roche Diagnostics
Indianapolis, IN, US
Received
March 31, 2022
Decision date
October 12, 2022
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MYF – Enzyme Linked Immunosorbent Assay, Herpes Simplex Virus, Hsv-2
Device class
Class II (moderate risk)
Regulation
21 CFR 866.3305
Specialty
Microbiology

Other 510(k)s with product code MYF

510(k)DeviceApplicantDecision
K243575ARCHITECT HSV-2 IgG, ARCHITECT HSV-2 IgG Calibrator, ARCHITECT HSV-2 IgG ControlsMYF · Traditional Biokit, S.A.02/12/2025SE
K181514SeraQuest HSV Type 2 Specific IgGMYF · Traditional Quest International, Inc.06/13/2019SE
K181334ADVIA Centaur Herpes-2 IgGMYF · Traditional Biokit, S.A.08/23/2018SE
K152353SeraQuest HSV Type 2 Specific IgGMYF · Traditional Quest International, Inc.05/13/2016SE
K103603Zeus Elisa HSV GG-2 Igg Test SystemMYF · Traditional Zeus Scientific, Inc.05/20/2011SE
K081687Liaison HSV-2 Type Specific Igg Assay, Control HSV-2 IggMYF · Traditional DiaSorin, Inc.11/10/2008SE
K061239Euroimmun ANTI-HSV-2 Elisa (Igg) and ANTI-HSV-1 Elisa (Igg) KitMYF · Traditional Euroimmun Us, LLC06/28/2007SE
K033106Captia HSV 2 Igg Type Specific Elisa KitMYF · Traditional Trinity Biotech USA07/13/2004SE
K993724HSV-2 Elisa Igg, Model EL0920GMYF · Traditional Mrl Diagnostics02/01/2000SE

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Questions and answers

When was Elecsys HSV-2 IgG (08948887160) cleared by the FDA?

Elecsys HSV-2 IgG (08948887160) (K220924) received a 510(k) decision of Substantially Equivalent on October 12, 2022, 195 days after the submission was received.

What is the product code of K220924?

The FDA product code is MYF – Enzyme Linked Immunosorbent Assay, Herpes Simplex Virus, Hsv-2, a Class II (moderate risk) device regulated under 21 CFR 866.3305.