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FDA 510(k)

QUICKTOX MULTIPLE DRUG DIPCARD

K-Number: K023489 · 2002-12-16

ApplicantBranan Medical Corp.
Decision Date2002-12-16
Product CodeDIO
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

QUICKTOX MULTIPLE DRUG DIPCARD is the device name listed in this FDA 510(k) record. The listed applicant is Branan Medical Corp.. It received FDA 510(k) clearance on 2002-12-16 under 510(k) number K023489. The device is classified under product code DIO. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUICKTOX MULTIPLE DRUG DIPCARD?

QUICKTOX MULTIPLE DRUG DIPCARD is a medical device that received FDA 510(k) clearance on 2002-12-16. The listed applicant is Branan Medical Corp.. The 510(k) number is K023489.

When did QUICKTOX MULTIPLE DRUG DIPCARD receive FDA 510(k) clearance?

QUICKTOX MULTIPLE DRUG DIPCARD received FDA 510(k) clearance on 2002-12-16, under 510(k) number K023489.

Who is the listed applicant for QUICKTOX MULTIPLE DRUG DIPCARD?

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

What is the FDA product code for QUICKTOX MULTIPLE DRUG DIPCARD?

The FDA product code for QUICKTOX MULTIPLE DRUG DIPCARD is DIO.

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Other records listing Branan Medical Corp. 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.

K122633TOXCUP DRUG SCREEN CUPK122752FASTECT II PPX DRUG SCREEN DIPSTICK, FASTECT II DRUG SCREEN DIPSTICK, QUICKTOX DRUG SCREEN DIPCARDK040203MONITECT MDMA DRUG SCREEN CASSETTE TEST, MODEL MC22; FASTECT II MDMA DRUG SCREEN DIPSTICK TEST, MODEL MF22K032057TOXCUP DRUG SCREEN CUP AMP/COC/MET/OPI/PCP/THCK030113MONITECT OXYCODONE DRUG SCREEN CASSETTE TEST, MODEL MC 23, FASTECT OXYCODONE DRUG SCREEN DIPSTICK TEST, MODEL MD23K022355QUICKTOX MULTIPLE DRUG DIPCARD COC/MET/THC/AMP/PCP/BZO/BAR/MTD/TCA, MODEL QT61

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Related Devices (Code: DIO)

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.

K213211Carolina Liquid Chemistries Cocaine and Cocaine Metabolite Enzyme Immunoassay (COCM) Test SystemCarolina Liquid Chemistries Corp.K211973DRI Cocaine Metabolite AssayMicrogenics CorporationK191638Pointe Scientific Cocaine Metabolite Enzyme ImmunoassayMedtest DXK181499DRI Cocaine Metabolite AssayMicrogenics CorporationK170293Emit II Plus Cocaine Metabolite AssaySiemens Healthcare Diagnostics, Inc.K163570Carolina Liquid Chemistries Cocaine and Cocaine Metabolite Test System (COCM)Carolina Liquid Chemistries Corporation

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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