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FDA 510(k)

N APOLIPOPROTEIN STANDARD SERUM

K-Number: K041870 · 2004-07-27

ApplicantDade Behring, Inc.
Decision Date2004-07-27
Product CodeJIX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

N APOLIPOPROTEIN STANDARD SERUM is the device name listed in this FDA 510(k) record. The listed applicant is Dade Behring, Inc.. It received FDA 510(k) clearance on 2004-07-27 under 510(k) number K041870. The device is classified under product code JIX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the N APOLIPOPROTEIN STANDARD SERUM?

N APOLIPOPROTEIN STANDARD SERUM is a medical device that received FDA 510(k) clearance on 2004-07-27. The listed applicant is Dade Behring, Inc.. The 510(k) number is K041870.

When did N APOLIPOPROTEIN STANDARD SERUM receive FDA 510(k) clearance?

N APOLIPOPROTEIN STANDARD SERUM received FDA 510(k) clearance on 2004-07-27, under 510(k) number K041870.

Who is the listed applicant for N APOLIPOPROTEIN STANDARD SERUM?

The FDA 510(k) record lists Dade Behring, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for N APOLIPOPROTEIN STANDARD SERUM?

The FDA product code for N APOLIPOPROTEIN STANDARD SERUM is JIX.

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Related Devices (Code: JIX)

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.

K161140VITROS Chemistry Products Calibrator Kit 3Ortho-Clinical Diagnostics, Inc.K133330C.F.A.S. PROTEINS, C.F.A.S. PAC, PRECICONTROL CLINCHEM MULTI 1 & 2, PRECINORM PROTEIN & PRECIPATH PROTEINRoche DiagnosticsK130765ELITECH CLINICAL SYSTEMS ELICAL 2; ELITECH CLINICAL SYSTEMS ELITROL I, ELITECH CLINICAL SYSTEMS ELITROL IIElitechgroupK123321DIMENSION CHEMISTRY III CALIBRATORYSiemens Healthcare DiagnosticsK123372ABBOTT LIPID MULTI CONSTITUENT CALIBRATORAbbott LaboratoriesK122398RAPIDPOINT 500 SYSTEM MEASUREMENT CARTRIDGE WITH CALIBRATORSSiemens Healthcare Diagnostics, 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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