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)

DRUG ABUSE DIPSTICKS

K-Number: K790805 · 1979-06-06

Decision Date1979-06-06
Product CodeDIT
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

DRUG ABUSE DIPSTICKS is the device name listed in this FDA 510(k) record. The listed applicant is Technical Resources, Inc.. It received FDA 510(k) clearance on 1979-06-06 under 510(k) number K790805. The device is classified under product code DIT. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DRUG ABUSE DIPSTICKS?

DRUG ABUSE DIPSTICKS is a medical device that received FDA 510(k) clearance on 1979-06-06. The listed applicant is Technical Resources, Inc.. The 510(k) number is K790805.

When did DRUG ABUSE DIPSTICKS receive FDA 510(k) clearance?

DRUG ABUSE DIPSTICKS received FDA 510(k) clearance on 1979-06-06, under 510(k) number K790805.

Who is the listed applicant for DRUG ABUSE DIPSTICKS?

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

What is the FDA product code for DRUG ABUSE DIPSTICKS?

The FDA product code for DRUG ABUSE DIPSTICKS is DIT.

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 Technical Resources, Inc. 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.

Related Devices (Code: DIT)

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.

↑