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FDA 510(k)

ADVIA Centaur Herpes-2 IgG

K-Number: K181334 · 2018-08-23

ApplicantBiokit, S.A.
Decision Date2018-08-23
Product CodeMYF
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ADVIA Centaur Herpes-2 IgG is the device name listed in this FDA 510(k) record. The listed applicant is Biokit, S.A.. It received FDA 510(k) clearance on 2018-08-23 under 510(k) number K181334. The device is classified under product code MYF. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADVIA Centaur Herpes-2 IgG?

ADVIA Centaur Herpes-2 IgG is a medical device that received FDA 510(k) clearance on 2018-08-23. The listed applicant is Biokit, S.A.. The 510(k) number is K181334.

When did ADVIA Centaur Herpes-2 IgG receive FDA 510(k) clearance?

ADVIA Centaur Herpes-2 IgG received FDA 510(k) clearance on 2018-08-23, under 510(k) number K181334.

Who is the listed applicant for ADVIA Centaur Herpes-2 IgG?

The FDA 510(k) record lists Biokit, S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ADVIA Centaur Herpes-2 IgG?

The FDA product code for ADVIA Centaur Herpes-2 IgG is MYF.

Other records listing Biokit, S.A. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 8 devices →

Related Devices (Code: MYF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.