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FDA 510(k)

MEDTOX OXYCODONE

K-Number: K060351 · 2006-05-12

ApplicantMedtox Diagnostics, Inc.
Decision Date2006-05-12
Product CodeDJG
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

MEDTOX OXYCODONE is the device name listed in this FDA 510(k) record. The listed applicant is Medtox Diagnostics, Inc.. It received FDA 510(k) clearance on 2006-05-12 under 510(k) number K060351. The device is classified under product code DJG. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDTOX OXYCODONE?

MEDTOX OXYCODONE is a medical device that received FDA 510(k) clearance on 2006-05-12. The listed applicant is Medtox Diagnostics, Inc.. The 510(k) number is K060351.

When did MEDTOX OXYCODONE receive FDA 510(k) clearance?

MEDTOX OXYCODONE received FDA 510(k) clearance on 2006-05-12, under 510(k) number K060351.

Who is the listed applicant for MEDTOX OXYCODONE?

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

What is the FDA product code for MEDTOX OXYCODONE?

The FDA product code for MEDTOX OXYCODONE is DJG.

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Other records listing Medtox Diagnostics, 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.

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Related Devices (Code: DJG)

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.

K252684Labcorp Fentanyl Urine Visual TestMedtox Diagnostics, Inc.K250741Evidence MultiSTAT DOA Urine MultiPlexRandox Laboratories LimitedK253082LZI Buprenorphine II Enzyme ImmunoassayLin-Zhi International, Inc.K252520SEFRIA™ Hydrocodone Oral FluidImmunalysis CorporationK251972Healgen® AccuFluor Fentanyl Fluorescence Immunoassay (FIA)Test Kit - Qualitative; Healgen® Immunofluorescence Analyzer (OG-H180)Healgen Scientific,, LLCK251634LZI Fentanyl III Enzyme ImmunoassayLin-Zhi International, Inc.

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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