ADVIA Centaur Herpes-1 IgG

FDA 510(k) K181333 · Biokit, S.A.

Substantially Equivalent

510(k) numberK181333

Submission

Device name
ADVIA Centaur Herpes-1 IgG
Applicant
Biokit, S.A.
Lliça D'Amunt, ES
Received
May 21, 2018
Decision date
August 23, 2018
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MXJ – Enzyme Linked Immunosorbent Assay, Herpes Simplex Virus, Hsv-1
Device class
Class II (moderate risk)
Regulation
21 CFR 866.3305
Specialty
Microbiology

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K162276SeraQuest Herpes Type 1 Specific IgGMXJ · Traditional Quest International, Inc.10/01/2016SE
K143236Theranos Herpes Simplex Virus-1 IgG AssayMXJ · Traditional Theranos, Inc.07/02/2015SE
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K120625Elecsys HSV-1 Igg Immunoassay Elecsys Precicontrol HSVMXJ · Traditional Roche Diagnostics07/25/2012SE
K120959Bioplex 2200 HSV-1 and HSV-2 Igg KitMXJ · Traditional Bio-Rad Laboratories06/22/2012SE
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Questions and answers

When was ADVIA Centaur Herpes-1 IgG cleared by the FDA?

ADVIA Centaur Herpes-1 IgG (K181333) received a 510(k) decision of Substantially Equivalent on August 23, 2018, 94 days after the submission was received.

What is the product code of K181333?

The FDA product code is MXJ – Enzyme Linked Immunosorbent Assay, Herpes Simplex Virus, Hsv-1, a Class II (moderate risk) device regulated under 21 CFR 866.3305.