Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

AT WORK DRUG TEST, MODEL 9147T AWT

K-Number: K010836 · 2001-04-11

ApplicantPhamatech
Decision Date2001-04-11
Product CodeLAF
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

AT WORK DRUG TEST, MODEL 9147T AWT is the device name listed in this FDA 510(k) record. The listed applicant is Phamatech. It received FDA 510(k) clearance on 2001-04-11 under 510(k) number K010836. The device is classified under product code LAF. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AT WORK DRUG TEST, MODEL 9147T AWT?

AT WORK DRUG TEST, MODEL 9147T AWT is a medical device that received FDA 510(k) clearance on 2001-04-11. The listed applicant is Phamatech. The 510(k) number is K010836.

When did AT WORK DRUG TEST, MODEL 9147T AWT receive FDA 510(k) clearance?

AT WORK DRUG TEST, MODEL 9147T AWT received FDA 510(k) clearance on 2001-04-11, under 510(k) number K010836.

Who is the listed applicant for AT WORK DRUG TEST, MODEL 9147T AWT?

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

What is the FDA product code for AT WORK DRUG TEST, MODEL 9147T AWT?

The FDA product code for AT WORK DRUG TEST, MODEL 9147T AWT is LAF.

Related Clinical Trials

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.

Other records listing Phamatech 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.

View all 47 devices →

Related Devices (Code: LAF)

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.

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.

↑