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FDA 510(k)

DMA MICROPROTEIN PROCEDURE

K-Number: K890868 · 1989-03-20

ApplicantData Medical Associates, Inc.
Decision Date1989-03-20
Product CodeCEK
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DMA MICROPROTEIN PROCEDURE is the device name listed in this FDA 510(k) record. The listed applicant is Data Medical Associates, Inc.. It received FDA 510(k) clearance on 1989-03-20 under 510(k) number K890868. The device is classified under product code CEK. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DMA MICROPROTEIN PROCEDURE?

DMA MICROPROTEIN PROCEDURE is a medical device that received FDA 510(k) clearance on 1989-03-20. The listed applicant is Data Medical Associates, Inc.. The 510(k) number is K890868.

When did DMA MICROPROTEIN PROCEDURE receive FDA 510(k) clearance?

DMA MICROPROTEIN PROCEDURE received FDA 510(k) clearance on 1989-03-20, under 510(k) number K890868.

Who is the listed applicant for DMA MICROPROTEIN PROCEDURE?

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

What is the FDA product code for DMA MICROPROTEIN PROCEDURE?

The FDA product code for DMA MICROPROTEIN PROCEDURE is CEK.

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Other records listing Data Medical Associates, 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.

K993098HDL-C/LDL-C CALIBRATOR, MODEL 1913-003K971113DMA TRIGLYCERIDES PROCEDURESK961919DMA GAMMA GLUTAMYLTRANSFERASE (GGT) PROCEDUREK955796IRON CALIBRATOR & CALIBRATION VERIFICATION SETK955302SERUM BICARBONATE/CARBON DIOXIDEK955300TOTAL BILIRUBIN PROCEDURE

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Related Devices (Code: CEK)

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.

K992846HICHEM TOTAL PROTEIN REAGENTElan Holdings, Inc.K973108TOTAL PROTEIN (MICRO) ASSAY, CATALOGUE NUMBER 450-50Diagnostic Chemicals , Ltd.K980042CARESIDE TOTAL PROTEINExigent Diagnostics, Inc.K971524TOTAL PROTEIN OR TPCarolina Liquid Chemistries Corp.K961864CSF/URINE TOTAL PROTEINTeco DiagnosticsK955905STC DIAGNOSTICS AUTO-LYTE URINARY PROTEIN ASSAYSolarcare Technologies Corp,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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