Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

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 the device name listed in this FDA 510(k) record. The listed applicant is Hoggan Scientific, LLC. It received FDA 510(k) clearance on 2017-03-09 under 510(k) 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. The listed applicant is Hoggan Scientific, LLC. The 510(k) number is K162412.

When did Hoggan Scientific® microFET2™ receive FDA 510(k) clearance?

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

Who is the listed applicant for Hoggan Scientific® microFET2™?

The FDA 510(k) record lists Hoggan Scientific, LLC as the applicant. This does not by itself establish the device manufacturer.

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.

↑