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FDA 510(k)

MODIFICATION TO SCOOPER DRUG/ADULTERATION TEST CUP

K-Number: K013124 · 2001-11-07

ApplicantBranan Medical Corp.
Decision Date2001-11-07
Product CodeDJJ
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO SCOOPER DRUG/ADULTERATION TEST CUP 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 2001-11-07 under 510(k) number K013124. The device is classified under product code DJJ. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION TO SCOOPER DRUG/ADULTERATION TEST CUP?

MODIFICATION TO SCOOPER DRUG/ADULTERATION TEST CUP is a medical device that received FDA 510(k) clearance on 2001-11-07. The listed applicant is Branan Medical Corp.. The 510(k) number is K013124.

When did MODIFICATION TO SCOOPER DRUG/ADULTERATION TEST CUP receive FDA 510(k) clearance?

MODIFICATION TO SCOOPER DRUG/ADULTERATION TEST CUP received FDA 510(k) clearance on 2001-11-07, under 510(k) number K013124.

Who is the listed applicant for MODIFICATION TO SCOOPER DRUG/ADULTERATION TEST CUP?

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 MODIFICATION TO SCOOPER DRUG/ADULTERATION TEST CUP?

The FDA product code for MODIFICATION TO SCOOPER DRUG/ADULTERATION TEST CUP is DJJ.

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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 MD23K023489QUICKTOX MULTIPLE DRUG DIPCARD

View all 13 devices →

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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