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FDA 510(k)

N CRP STANDARD SY

K-Number: K962406 · 1996-07-16

ApplicantBehring Diagnostics, Inc.
Decision Date1996-07-16
Product CodeJIX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

N CRP STANDARD SY is the device name listed in this FDA 510(k) record. The listed applicant is Behring Diagnostics, Inc.. It received FDA 510(k) clearance on 1996-07-16 under 510(k) number K962406. 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 CRP STANDARD SY?

N CRP STANDARD SY is a medical device that received FDA 510(k) clearance on 1996-07-16. The listed applicant is Behring Diagnostics, Inc.. The 510(k) number is K962406.

When did N CRP STANDARD SY receive FDA 510(k) clearance?

N CRP STANDARD SY received FDA 510(k) clearance on 1996-07-16, under 510(k) number K962406.

Who is the listed applicant for N CRP STANDARD SY?

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

What is the FDA product code for N CRP STANDARD SY?

The FDA product code for N CRP STANDARD SY is JIX.

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Other records listing Behring Diagnostics, Inc. 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.

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Related Devices (Code: JIX)

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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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