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FDA 510(k)

PSYCHEMEDICS MICROPLATE EIA FOR OXYCODONE IN HAIR

K-Number: K123799 · 2013-02-08

Decision Date2013-02-08
Product CodeDJG
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

PSYCHEMEDICS MICROPLATE EIA FOR OXYCODONE IN HAIR is the device name listed in this FDA 510(k) record. The listed applicant is Psychemedics Corp.. It received FDA 510(k) clearance on 2013-02-08 under 510(k) number K123799. 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 PSYCHEMEDICS MICROPLATE EIA FOR OXYCODONE IN HAIR?

PSYCHEMEDICS MICROPLATE EIA FOR OXYCODONE IN HAIR is a medical device that received FDA 510(k) clearance on 2013-02-08. The listed applicant is Psychemedics Corp.. The 510(k) number is K123799.

When did PSYCHEMEDICS MICROPLATE EIA FOR OXYCODONE IN HAIR receive FDA 510(k) clearance?

PSYCHEMEDICS MICROPLATE EIA FOR OXYCODONE IN HAIR received FDA 510(k) clearance on 2013-02-08, under 510(k) number K123799.

Who is the listed applicant for PSYCHEMEDICS MICROPLATE EIA FOR OXYCODONE IN HAIR?

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

What is the FDA product code for PSYCHEMEDICS MICROPLATE EIA FOR OXYCODONE IN HAIR?

The FDA product code for PSYCHEMEDICS MICROPLATE EIA FOR OXYCODONE IN HAIR is DJG.

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 Psychemedics Corp. 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 12 devices →

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.

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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