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FDA 510(k)

BioCode Gastrointestinal Pathogen Panel (GPP)

K-Number: K242877 · 2025-01-10

Decision Date2025-01-10
Product CodePCH
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

BioCode Gastrointestinal Pathogen Panel (GPP) is a medical device manufactured by Applied BioCode, Inc.. It received FDA 510(k) clearance on 2025-01-10 under approval number K242877. The device is classified under product code PCH. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BioCode Gastrointestinal Pathogen Panel (GPP)?

BioCode Gastrointestinal Pathogen Panel (GPP) is a medical device that received FDA 510(k) clearance on 2025-01-10. It is manufactured by Applied BioCode, Inc.. The 510(k) number is K242877.

When was BioCode Gastrointestinal Pathogen Panel (GPP) approved by the FDA?

BioCode Gastrointestinal Pathogen Panel (GPP) received FDA 510(k) clearance on 2025-01-10, under approval number K242877.

What company makes BioCode Gastrointestinal Pathogen Panel (GPP)?

BioCode Gastrointestinal Pathogen Panel (GPP) is manufactured by Applied BioCode, Inc..

What is the FDA product code for BioCode Gastrointestinal Pathogen Panel (GPP)?

The FDA product code for BioCode Gastrointestinal Pathogen Panel (GPP) is PCH.

Related Clinical Trials

Other Devices by Applied BioCode, Inc.

Related Devices (Code: PCH)

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.