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FDA 510(k)

Portable Mesh Nebulizer

K-Number: K182906 · 2020-09-27

ApplicantFeellife Health, Inc.
Decision Date2020-09-27
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

Portable Mesh Nebulizer is a medical device manufactured by Feellife Health, Inc.. It received FDA 510(k) clearance on 2020-09-27 under approval number K182906. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Portable Mesh Nebulizer?

Portable Mesh Nebulizer is a medical device that received FDA 510(k) clearance on 2020-09-27. It is manufactured by Feellife Health, Inc.. The 510(k) number is K182906.

When was Portable Mesh Nebulizer approved by the FDA?

Portable Mesh Nebulizer received FDA 510(k) clearance on 2020-09-27, under approval number K182906.

What company makes Portable Mesh Nebulizer?

Portable Mesh Nebulizer is manufactured by Feellife Health, Inc..

What is the FDA product code for Portable Mesh Nebulizer?

The FDA product code for Portable Mesh Nebulizer is CAF.

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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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