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FDA 510(k)

DU PONT LIQUID MULTI-ANALYTE CALIBRATOR

K-Number: K864909 · 1987-02-13

ApplicantE.I. Dupont DE Nemours & Co., Inc.
Decision Date1987-02-13
Product CodeJIX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DU PONT LIQUID MULTI-ANALYTE CALIBRATOR is the device name listed in this FDA 510(k) record. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. It received FDA 510(k) clearance on 1987-02-13 under 510(k) number K864909. 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 DU PONT LIQUID MULTI-ANALYTE CALIBRATOR?

DU PONT LIQUID MULTI-ANALYTE CALIBRATOR is a medical device that received FDA 510(k) clearance on 1987-02-13. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K864909.

When did DU PONT LIQUID MULTI-ANALYTE CALIBRATOR receive FDA 510(k) clearance?

DU PONT LIQUID MULTI-ANALYTE CALIBRATOR received FDA 510(k) clearance on 1987-02-13, under 510(k) number K864909.

Who is the listed applicant for DU PONT LIQUID MULTI-ANALYTE CALIBRATOR?

The FDA 510(k) record lists E.I. Dupont DE Nemours & Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DU PONT LIQUID MULTI-ANALYTE CALIBRATOR?

The FDA product code for DU PONT LIQUID MULTI-ANALYTE CALIBRATOR is JIX.

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Other records listing E.I. Dupont DE Nemours & Co., 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.

K951851ALLIANCE CYTOMEGALOVIRUS IMMEDIATE EARLY ANTIGEN DIRECT IMMUNOFLUORESCENCE ASSAYK953724CRONEX RADIATION THERAPY CASSETTEK953725CRONEX RADIATION THERAPY VERIFICATION CASSETTEK951441DUPONT ACA DIGOXIN (DGN A) METHODK950137URINE BARBITURATES SCREEN FLEX(TM) REAGENT CARTRIDGEK950136URINE OPIATES SCREEN FLEX(TM) REAGENT CARTRIDGE

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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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