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FDA 510(k)

DUPONT DIMENSION TOTAL PROTEIN METHOD

K-Number: K950920 · 1995-08-11

ApplicantDupont Medical Products
Decision Date1995-08-11
Product CodeCEK
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DUPONT DIMENSION TOTAL PROTEIN METHOD is the device name listed in this FDA 510(k) record. The listed applicant is Dupont Medical Products. It received FDA 510(k) clearance on 1995-08-11 under 510(k) number K950920. 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 DUPONT DIMENSION TOTAL PROTEIN METHOD?

DUPONT DIMENSION TOTAL PROTEIN METHOD is a medical device that received FDA 510(k) clearance on 1995-08-11. The listed applicant is Dupont Medical Products. The 510(k) number is K950920.

When did DUPONT DIMENSION TOTAL PROTEIN METHOD receive FDA 510(k) clearance?

DUPONT DIMENSION TOTAL PROTEIN METHOD received FDA 510(k) clearance on 1995-08-11, under 510(k) number K950920.

Who is the listed applicant for DUPONT DIMENSION TOTAL PROTEIN METHOD?

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

What is the FDA product code for DUPONT DIMENSION TOTAL PROTEIN METHOD?

The FDA product code for DUPONT DIMENSION TOTAL PROTEIN METHOD is CEK.

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Other records listing Dupont Medical Products 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.

K952815DUPONT LIPASE CALIBRATORK952816LIPASE FLEX REAGENT CARTRIDGEK952412DUPONT ACA(R) URINE DRUGE OS ABUSE CONTROLK945280DUPONT DIMENSION C-REACTIVE PROTEIN METHODK944932PHENOBARBITAL FLEX REAGENT CARTRIDGEK941050DUPONT ACA STAR

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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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