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FDA 510(k)

Hoggan Scientific® microFET2™

K-Number: K162412 · 2017-03-09

ApplicantHoggan Scientific, LLC
Decision Date2017-03-09
Product CodeLBB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Hoggan Scientific® microFET2™ is a medical device manufactured by Hoggan Scientific, LLC. It received FDA 510(k) clearance on 2017-03-09 under approval number K162412. The device is classified under product code LBB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Hoggan Scientific® microFET2™?

Hoggan Scientific® microFET2™ is a medical device that received FDA 510(k) clearance on 2017-03-09. It is manufactured by Hoggan Scientific, LLC. The 510(k) number is K162412.

When was Hoggan Scientific® microFET2™ approved by the FDA?

Hoggan Scientific® microFET2™ received FDA 510(k) clearance on 2017-03-09, under approval number K162412.

What company makes Hoggan Scientific® microFET2™?

Hoggan Scientific® microFET2™ is manufactured by Hoggan Scientific, LLC.

What is the FDA product code for Hoggan Scientific® microFET2™?

The FDA product code for Hoggan Scientific® microFET2™ is LBB.

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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