ADVIA Centaur Herpes-2 IgG

FDA 510(k) K181334 · Biokit, S.A.

Substantially Equivalent

510(k) numberK181334

Submission

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

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Questions and answers

When was ADVIA Centaur Herpes-2 IgG cleared by the FDA?

ADVIA Centaur Herpes-2 IgG (K181334) 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 K181334?

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.