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FDA 510(k)

DOUMENT TM LINEARITY TEST STANDARDS

K-Number: K843947 · 1984-10-17

ApplicantCasco Standards
Decision Date1984-10-17
Product CodeJIX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DOUMENT TM LINEARITY TEST STANDARDS is the device name listed in this FDA 510(k) record. The listed applicant is Casco Standards. It received FDA 510(k) clearance on 1984-10-17 under 510(k) number K843947. 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 DOUMENT TM LINEARITY TEST STANDARDS?

DOUMENT TM LINEARITY TEST STANDARDS is a medical device that received FDA 510(k) clearance on 1984-10-17. The listed applicant is Casco Standards. The 510(k) number is K843947.

When did DOUMENT TM LINEARITY TEST STANDARDS receive FDA 510(k) clearance?

DOUMENT TM LINEARITY TEST STANDARDS received FDA 510(k) clearance on 1984-10-17, under 510(k) number K843947.

Who is the listed applicant for DOUMENT TM LINEARITY TEST STANDARDS?

The FDA 510(k) record lists Casco Standards as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DOUMENT TM LINEARITY TEST STANDARDS?

The FDA product code for DOUMENT TM LINEARITY TEST STANDARDS 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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