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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 the device name listed in this FDA 510(k) record. The listed applicant is Feellife Health, Inc.. It received FDA 510(k) clearance on 2020-09-27 under 510(k) 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. The listed applicant is Feellife Health, Inc.. The 510(k) number is K182906.

When did Portable Mesh Nebulizer receive FDA 510(k) clearance?

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

Who is the listed applicant for Portable Mesh Nebulizer?

The FDA 510(k) record lists Feellife Health, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Portable Mesh Nebulizer?

The FDA product code for Portable Mesh Nebulizer is CAF.

Other records listing Feellife Health, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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.

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