HOMED Mesh Nebulizer
K-Number: K170886 · 2018-06-21
Decision Date2018-06-21
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent
Device Summary
HOMED Mesh Nebulizer is a medical device manufactured by Shenzhen Homed Medical Device Co., Ltd.. It received FDA 510(k) clearance on 2018-06-21 under approval number K170886. 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 HOMED Mesh Nebulizer?
HOMED Mesh Nebulizer is a medical device that received FDA 510(k) clearance on 2018-06-21. It is manufactured by Shenzhen Homed Medical Device Co., Ltd.. The 510(k) number is K170886.
When was HOMED Mesh Nebulizer approved by the FDA?
HOMED Mesh Nebulizer received FDA 510(k) clearance on 2018-06-21, under approval number K170886.
What company makes HOMED Mesh Nebulizer?
HOMED Mesh Nebulizer is manufactured by Shenzhen Homed Medical Device Co., Ltd..
What is the FDA product code for HOMED Mesh Nebulizer?
The FDA product code for HOMED Mesh Nebulizer is CAF.
Other Devices by Shenzhen Homed Medical Device Co., Ltd.
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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.