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FDA 510(k)

BRANAN MEDICAL CORPORARTION MONITECT THC DRUG SCREEN TEST

K-Number: K002263 · 2000-11-27

ApplicantBranan Medical Corp.
Decision Date2000-11-27
Product CodeLDJ
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

BRANAN MEDICAL CORPORARTION MONITECT THC DRUG SCREEN TEST 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 2000-11-27 under 510(k) number K002263. The device is classified under product code LDJ. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRANAN MEDICAL CORPORARTION MONITECT THC DRUG SCREEN TEST?

BRANAN MEDICAL CORPORARTION MONITECT THC DRUG SCREEN TEST is a medical device that received FDA 510(k) clearance on 2000-11-27. The listed applicant is Branan Medical Corp.. The 510(k) number is K002263.

When did BRANAN MEDICAL CORPORARTION MONITECT THC DRUG SCREEN TEST receive FDA 510(k) clearance?

BRANAN MEDICAL CORPORARTION MONITECT THC DRUG SCREEN TEST received FDA 510(k) clearance on 2000-11-27, under 510(k) number K002263.

Who is the listed applicant for BRANAN MEDICAL CORPORARTION MONITECT THC DRUG SCREEN TEST?

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 BRANAN MEDICAL CORPORARTION MONITECT THC DRUG SCREEN TEST?

The FDA product code for BRANAN MEDICAL CORPORARTION MONITECT THC DRUG SCREEN TEST is LDJ.

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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

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Related Devices (Code: LDJ)

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.

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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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