可穿戴式乳腺泵，型号S18
K号: K232774 · 2024-06-06
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决定日期2024-06-06
产品代码HGX
咨询委员会OB
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决定实质等同
器械摘要
Wearable Breast Pump,Model S18 is the device name listed in this FDA 510(k) record. The listed applicant is Ningbo Dearevery Electronic Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-06-06 under 510(k) number K232774. The device is classified under product code HGX. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Wearable Breast Pump,Model S18?
Wearable Breast Pump,Model S18 is a medical device that received FDA 510(k) clearance on 2024-06-06. The listed applicant is Ningbo Dearevery Electronic Technology Co., Ltd.. The 510(k) number is K232774.
When did Wearable Breast Pump,Model S18 receive FDA 510(k) clearance?
Wearable Breast Pump,Model S18 received FDA 510(k) clearance on 2024-06-06, under 510(k) number K232774.
Who is the listed applicant for Wearable Breast Pump,Model S18?
The FDA 510(k) record lists Ningbo Dearevery Electronic Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Wearable Breast Pump,Model S18?
The FDA product code for Wearable Breast Pump,Model S18 is HGX.
相关临床试验
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。
相关器械（代码：HGX）
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。
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官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。
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