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FDA 510(k)

SEFRIA Oxycodone Oral Fluid Enzyme Immunoassay

K-Number: K203564 · 2021-12-22

ApplicantImmunalysis Corporation
Decision Date2021-12-22
Product CodeDJG
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

SEFRIA Oxycodone Oral Fluid Enzyme Immunoassay is a medical device manufactured by Immunalysis Corporation. It received FDA 510(k) clearance on 2021-12-22 under approval number K203564. 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 SEFRIA Oxycodone Oral Fluid Enzyme Immunoassay?

SEFRIA Oxycodone Oral Fluid Enzyme Immunoassay is a medical device that received FDA 510(k) clearance on 2021-12-22. It is manufactured by Immunalysis Corporation. The 510(k) number is K203564.

When was SEFRIA Oxycodone Oral Fluid Enzyme Immunoassay approved by the FDA?

SEFRIA Oxycodone Oral Fluid Enzyme Immunoassay received FDA 510(k) clearance on 2021-12-22, under approval number K203564.

What company makes SEFRIA Oxycodone Oral Fluid Enzyme Immunoassay?

SEFRIA Oxycodone Oral Fluid Enzyme Immunoassay is manufactured by Immunalysis Corporation.

What is the FDA product code for SEFRIA Oxycodone Oral Fluid Enzyme Immunoassay?

The FDA product code for SEFRIA Oxycodone Oral Fluid Enzyme Immunoassay is DJG.

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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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