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

FDA 510(k)

Moxxly Flow Collection System

K-Number: K170722 · 2017-08-28

ApplicantMoxxly, Inc.
Decision Date2017-08-28
Product CodeHGX
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Moxxly Flow Collection System is a medical device manufactured by Moxxly, Inc.. It received FDA 510(k) clearance on 2017-08-28 under approval number K170722. The device is classified under product code HGX. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Moxxly Flow Collection System?

Moxxly Flow Collection System is a medical device that received FDA 510(k) clearance on 2017-08-28. It is manufactured by Moxxly, Inc.. The 510(k) number is K170722.

When was Moxxly Flow Collection System approved by the FDA?

Moxxly Flow Collection System received FDA 510(k) clearance on 2017-08-28, under approval number K170722.

What company makes Moxxly Flow Collection System?

Moxxly Flow Collection System is manufactured by Moxxly, Inc..

What is the FDA product code for Moxxly Flow Collection System?

The FDA product code for Moxxly Flow Collection System is HGX.

Related Clinical Trials

Related Devices (Code: HGX)

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.