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FDA 510(k)

MDI QUIK TEST NARCOTICS DRUG SCREEN

K-Number: K853140 · 1986-03-03

ApplicantMedical Diagnostics, Ca.
Decision Date1986-03-03
Product CodeDNK
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

MDI QUIK TEST NARCOTICS DRUG SCREEN is the device name listed in this FDA 510(k) record. The listed applicant is Medical Diagnostics, Ca.. It received FDA 510(k) clearance on 1986-03-03 under 510(k) number K853140. The device is classified under product code DNK. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MDI QUIK TEST NARCOTICS DRUG SCREEN?

MDI QUIK TEST NARCOTICS DRUG SCREEN is a medical device that received FDA 510(k) clearance on 1986-03-03. The listed applicant is Medical Diagnostics, Ca.. The 510(k) number is K853140.

When did MDI QUIK TEST NARCOTICS DRUG SCREEN receive FDA 510(k) clearance?

MDI QUIK TEST NARCOTICS DRUG SCREEN received FDA 510(k) clearance on 1986-03-03, under 510(k) number K853140.

Who is the listed applicant for MDI QUIK TEST NARCOTICS DRUG SCREEN?

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

What is the FDA product code for MDI QUIK TEST NARCOTICS DRUG SCREEN?

The FDA product code for MDI QUIK TEST NARCOTICS DRUG SCREEN is DNK.

Related Clinical Trials

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Other records listing Medical Diagnostics, Ca. 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.

K843900FOCUSCOPE UNIVERSAL SYSTEMK843343MEDICA IIF-ANTI-THYROID ANTIBODY TESTK831100MEDICA IIF-MULTIPLE ANTIBODY TEST KIT

Related Devices (Code: DNK)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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