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FDA 510(k)

MULTI-ANALYTE DETECTION SYSTEMS

K-Number: K112810 · 2011-10-26

ApplicantBio-Rad Laboratories
Decision Date2011-10-26
Product CodeNHX
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

MULTI-ANALYTE DETECTION SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad Laboratories. It received FDA 510(k) clearance on 2011-10-26 under 510(k) number K112810. The device is classified under product code NHX. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTI-ANALYTE DETECTION SYSTEMS?

MULTI-ANALYTE DETECTION SYSTEMS is a medical device that received FDA 510(k) clearance on 2011-10-26. The listed applicant is Bio-Rad Laboratories. The 510(k) number is K112810.

When did MULTI-ANALYTE DETECTION SYSTEMS receive FDA 510(k) clearance?

MULTI-ANALYTE DETECTION SYSTEMS received FDA 510(k) clearance on 2011-10-26, under 510(k) number K112810.

Who is the listed applicant for MULTI-ANALYTE DETECTION SYSTEMS?

The FDA 510(k) record lists Bio-Rad Laboratories as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULTI-ANALYTE DETECTION SYSTEMS?

The FDA product code for MULTI-ANALYTE DETECTION SYSTEMS is NHX.

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Related Devices (Code: NHX)

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.

K153551ADVIA Centaur Anti-CCP IgG (aCCP) assay including Reagents and Calibrators, Quality Controls and Master Curve Materials.Axis-Shield Diagnostics LimitedK121576IMMULITE 2000 ANTI-CCP IGG ASSAYSiemens Healthcare Diagnostics, Inc.K110296AXIS-SHIELD ANTI-CCPAxis-Shield Diagnostics, Ltd.K093908CCPOINTEuro-Diagnostica ABK093954BIOPLEX 2200 ANTI-CCP KIT ON THE BIOPLEX 2200 MULTI-ANALYTE DETECTION SYSTEMBio-Rad LaboratoriesK090753THERATEST EL-ANTI-CCP/2Theratest Laboratories, Inc.

Official Source

View on FDA Database →

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

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