FDA 510(k)

雾化器

K号: K212395 · 2022-03-25

申请人Shenzhen Homed Medical Device Co., Ltd.

决定日期2022-03-25

产品代码CAF

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决定实质等同

器械摘要

Nebulizer is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Homed Medical Device Co., Ltd.. It received FDA 510(k) clearance on 2022-03-25 under 510(k) number K212395. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Nebulizer?

Nebulizer is a medical device that received FDA 510(k) clearance on 2022-03-25. The listed applicant is Shenzhen Homed Medical Device Co., Ltd.. The 510(k) number is K212395.

When did Nebulizer receive FDA 510(k) clearance?

Nebulizer received FDA 510(k) clearance on 2022-03-25, under 510(k) number K212395.

Who is the listed applicant for Nebulizer?

The FDA 510(k) record lists Shenzhen Homed Medical Device Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Nebulizer?

The FDA product code for Nebulizer is CAF.

列明Shenzhen Homed Medical Device Co., Ltd.为申报人的其他记录

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

K252616便携式制氧机（JLO-190P）K170886HOMED 网状雾化器 K161586JLN-23XX系列活塞压缩雾化器（型号为JLN-2300AS、JLN-2301AS、JLN-2317AS和JLN-2320AS）

相关器械（代码：CAF）

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

K254171网状雾化器（UN204）；网状雾化器（UN205）；网状雾化器（UN209）；网状雾化器（UN210）Shenzhen Mericonn Technology Co., Ltd.K260270FindAir ONE 用于 pMDI (FAO-MDI-V12-GRE-001)FindAir Sp. z o.o.K251572eRapid带eTrack系统Pari Respiratory Equipment, Inc.K251659Mesh Nebulizer (H6)Qingdao Future Medical Technology Co., Ltd.K244035便携式网状雾化器（JM821）Shenzhen Jermei Medical Device Technology Co., Ltd.K243468压缩机雾化器（NB-1100）；压缩机雾化器（NB-1101）；压缩机雾化器（NB-1102）；压缩机雾化器（NB-1103）Joytech Healthcare Co. , Ltd.

官方来源

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