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FDA 510(k)

CONTOX DURG CONTROL

K-Number: K830492 · 1983-03-11

ApplicantKaulson Laboratories, Inc.
Decision Date1983-03-11
Product CodeDIF
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

CONTOX DURG CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Kaulson Laboratories, Inc.. It received FDA 510(k) clearance on 1983-03-11 under 510(k) number K830492. 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 CONTOX DURG CONTROL?

CONTOX DURG CONTROL is a medical device that received FDA 510(k) clearance on 1983-03-11. The listed applicant is Kaulson Laboratories, Inc.. The 510(k) number is K830492.

When did CONTOX DURG CONTROL receive FDA 510(k) clearance?

CONTOX DURG CONTROL received FDA 510(k) clearance on 1983-03-11, under 510(k) number K830492.

Who is the listed applicant for CONTOX DURG CONTROL?

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

What is the FDA product code for CONTOX DURG CONTROL?

The FDA product code for CONTOX DURG CONTROL is DIF.

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Other records listing Kaulson Laboratories, 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.

K830493PROTOPORPHYRIN ZN CONTROLK830494CONTOX DRUG SCREEN CONTROLK830234CONTOX HEAVYMETALS CONTROL

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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