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FDA 510(k)

DUPONT ACA(R) URINE DRUGE OS ABUSE CONTROL

K-Number: K952412 · 1995-06-23

ApplicantDupont Medical Products
Decision Date1995-06-23
Product CodeDIF
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

DUPONT ACA(R) URINE DRUGE OS ABUSE CONTROL 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 1995-06-23 under 510(k) number K952412. The device is classified under product code DIF. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUPONT ACA(R) URINE DRUGE OS ABUSE CONTROL?

DUPONT ACA(R) URINE DRUGE OS ABUSE CONTROL is a medical device that received FDA 510(k) clearance on 1995-06-23. The listed applicant is Dupont Medical Products. The 510(k) number is K952412.

When did DUPONT ACA(R) URINE DRUGE OS ABUSE CONTROL receive FDA 510(k) clearance?

DUPONT ACA(R) URINE DRUGE OS ABUSE CONTROL received FDA 510(k) clearance on 1995-06-23, under 510(k) number K952412.

Who is the listed applicant for DUPONT ACA(R) URINE DRUGE OS ABUSE CONTROL?

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 ACA(R) URINE DRUGE OS ABUSE CONTROL?

The FDA product code for DUPONT ACA(R) URINE DRUGE OS ABUSE CONTROL is DIF.

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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 CALIBRATORK950920DUPONT DIMENSION TOTAL PROTEIN METHODK952816LIPASE FLEX REAGENT CARTRIDGEK945280DUPONT DIMENSION C-REACTIVE PROTEIN METHODK944932PHENOBARBITAL FLEX REAGENT CARTRIDGEK941050DUPONT ACA STAR

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Related Devices (Code: DIF)

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.

K153474Detectabuse Liquid Control Urine, Detectabuse Stat-Skreen Liquid Control Urine, Detectabuse Liquid Control Urine, AU/NZ, Detectabuse Liquid Control Urine, Immunoassay Series, Detectabuse Liquid Control Urine, GC/MS and Confirm seriesBiochemical Diagnostics, Inc.K132688SALIVABUSE LIQUID ORAL FLUID CONTROL, SALIVABUSE LIQUID ORAL FLUID CONTROL, AU/NZBiochemical Diagnostics, Inc.K132174MULTICHEM WBTTechno-Path Manufacturing , Ltd.K121122DETECTABUSE LIQUID CONTROL, DETECTABUSE STAT-SKREEN LIQUID CONTROLBiochemical Diagnostic, Inc.K121143LIQUICHEK WHOLE BLOOD IMMUNOSUPPRESSANT CONTROL TILEVEL (1,2 AND 3)Bio-Rad LaboratoriesK120504LIQUICHEK URINE TOXICOLOGY CONTROL, S10 & S10 MINIPAK, LIQUICHEK URINE TOXICOLOGY CONTROL, LEVEL S20 & LEVEL S20 MINIPAKBio-Rad Laboratories, 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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