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FDA 510(k)

TOXCUP DRUG SCREEN CUP AMP/COC/MET/OPI/PCP/THC

K-Number: K032057 · 2003-08-21

ApplicantBranan Medical Corp.
Decision Date2003-08-21
Product CodeDIO
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

TOXCUP DRUG SCREEN CUP AMP/COC/MET/OPI/PCP/THC 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 2003-08-21 under 510(k) number K032057. 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 TOXCUP DRUG SCREEN CUP AMP/COC/MET/OPI/PCP/THC?

TOXCUP DRUG SCREEN CUP AMP/COC/MET/OPI/PCP/THC is a medical device that received FDA 510(k) clearance on 2003-08-21. The listed applicant is Branan Medical Corp.. The 510(k) number is K032057.

When did TOXCUP DRUG SCREEN CUP AMP/COC/MET/OPI/PCP/THC receive FDA 510(k) clearance?

TOXCUP DRUG SCREEN CUP AMP/COC/MET/OPI/PCP/THC received FDA 510(k) clearance on 2003-08-21, under 510(k) number K032057.

Who is the listed applicant for TOXCUP DRUG SCREEN CUP AMP/COC/MET/OPI/PCP/THC?

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 TOXCUP DRUG SCREEN CUP AMP/COC/MET/OPI/PCP/THC?

The FDA product code for TOXCUP DRUG SCREEN CUP AMP/COC/MET/OPI/PCP/THC 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 MF22K030113MONITECT OXYCODONE DRUG SCREEN CASSETTE TEST, MODEL MC 23, FASTECT OXYCODONE DRUG SCREEN DIPSTICK TEST, MODEL MD23K023489QUICKTOX MULTIPLE DRUG DIPCARDK022355QUICKTOX MULTIPLE DRUG DIPCARD COC/MET/THC/AMP/PCP/BZO/BAR/MTD/TCA, MODEL QT61

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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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