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FDA 510(k)

Monarch Airway Clearance System

K-Number: K173603 · 2018-10-24

Decision Date2018-10-24
Product CodeBYI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

Monarch Airway Clearance System is a medical device manufactured by Hill-Rom Holdings, Inc.. It received FDA 510(k) clearance on 2018-10-24 under approval number K173603. The device is classified under product code BYI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Monarch Airway Clearance System?

Monarch Airway Clearance System is a medical device that received FDA 510(k) clearance on 2018-10-24. It is manufactured by Hill-Rom Holdings, Inc.. The 510(k) number is K173603.

When was Monarch Airway Clearance System approved by the FDA?

Monarch Airway Clearance System received FDA 510(k) clearance on 2018-10-24, under approval number K173603.

What company makes Monarch Airway Clearance System?

Monarch Airway Clearance System is manufactured by Hill-Rom Holdings, Inc..

What is the FDA product code for Monarch Airway Clearance System?

The FDA product code for Monarch Airway Clearance System is BYI.

Related Clinical Trials

Related Devices (Code: BYI)

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.