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)

MetaNeb 4 System

K-Number: K151689 · 2016-03-17

Decision Date2016-03-17
Product CodeNHJ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MetaNeb 4 System is a medical device manufactured by Hill-Rom Services Pte, Ltd.. It received FDA 510(k) clearance on 2016-03-17 under approval number K151689. The device is classified under product code NHJ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MetaNeb 4 System?

MetaNeb 4 System is a medical device that received FDA 510(k) clearance on 2016-03-17. It is manufactured by Hill-Rom Services Pte, Ltd.. The 510(k) number is K151689.

When was MetaNeb 4 System approved by the FDA?

MetaNeb 4 System received FDA 510(k) clearance on 2016-03-17, under approval number K151689.

What company makes MetaNeb 4 System?

MetaNeb 4 System is manufactured by Hill-Rom Services Pte, Ltd..

What is the FDA product code for MetaNeb 4 System?

The FDA product code for MetaNeb 4 System is NHJ.

Other Devices by Hill-Rom Services Pte, Ltd.

Related Devices (Code: NHJ)

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.