FDA 510(k)

ACA URINE DRUGS OF ABUSE CONTROL

K-Number: K873539 · 1987-10-07

ApplicantE.I. Dupont DE Nemours & Co., Inc.

Decision Date1987-10-07

Product CodeDIF

Advisory CommitteeTX

DecisionSubstantially Equivalent

Device Summary

ACA URINE DRUGS OF ABUSE CONTROL 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 1987-10-07 under 510(k) number K873539. 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 ACA URINE DRUGS OF ABUSE CONTROL?

ACA URINE DRUGS OF ABUSE CONTROL is a medical device that received FDA 510(k) clearance on 1987-10-07. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K873539.

When did ACA URINE DRUGS OF ABUSE CONTROL receive FDA 510(k) clearance?

ACA URINE DRUGS OF ABUSE CONTROL received FDA 510(k) clearance on 1987-10-07, under 510(k) number K873539.

Who is the listed applicant for ACA URINE DRUGS OF ABUSE CONTROL?

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 ACA URINE DRUGS OF ABUSE CONTROL?

The FDA product code for ACA URINE DRUGS OF ABUSE CONTROL is DIF.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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

K951851ALLIANCE CYTOMEGALOVIRUS IMMEDIATE EARLY ANTIGEN DIRECT IMMUNOFLUORESCENCE ASSAY K953724CRONEX RADIATION THERAPY CASSETTE K953725CRONEX RADIATION THERAPY VERIFICATION CASSETTE K951441DUPONT ACA DIGOXIN (DGN A) METHOD K950137URINE BARBITURATES SCREEN FLEX(TM) REAGENT CARTRIDGE K950136URINE OPIATES SCREEN FLEX(TM) REAGENT CARTRIDGE

View all 253 devices →

Related Devices (Code: DIF)

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 Laboratories K120504LIQUICHEK 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.