FDA 510(k)

BRANAN MEDICAL CORPORATION MONITECT BARBITURATES DRUG SCREEN TEST

K-Number: K002337 · 2000-11-22

Decision Date2000-11-22

Product CodeDIS

Advisory CommitteeTX

DecisionSubstantially Equivalent

Device Summary

BRANAN MEDICAL CORPORATION MONITECT BARBITURATES DRUG SCREEN TEST is the device name listed in this FDA 510(k) record. The listed applicant is Branan Medical Corporation. It received FDA 510(k) clearance on 2000-11-22 under 510(k) number K002337. The device is classified under product code DIS. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRANAN MEDICAL CORPORATION MONITECT BARBITURATES DRUG SCREEN TEST?

BRANAN MEDICAL CORPORATION MONITECT BARBITURATES DRUG SCREEN TEST is a medical device that received FDA 510(k) clearance on 2000-11-22. The listed applicant is Branan Medical Corporation. The 510(k) number is K002337.

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

BRANAN MEDICAL CORPORATION MONITECT BARBITURATES DRUG SCREEN TEST received FDA 510(k) clearance on 2000-11-22, under 510(k) number K002337.

Who is the listed applicant for BRANAN MEDICAL CORPORATION MONITECT BARBITURATES DRUG SCREEN TEST?

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

What is the FDA product code for BRANAN MEDICAL CORPORATION MONITECT BARBITURATES DRUG SCREEN TEST?

The FDA product code for BRANAN MEDICAL CORPORATION MONITECT BARBITURATES DRUG SCREEN TEST is DIS.

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Other records listing Branan Medical Corporation as applicant

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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.