FDA 510(k)

可穿戴式乳腺泵（型号S10）

K号: K220309 · 2022-06-27

申请人Shenzhen Lutejiacheng Technology Co., Ltd.

决定日期2022-06-27

产品代码HGX

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决定实质等同

器械摘要

Wearable Breast Pump (Model S10) is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Lutejiacheng Technology Co., Ltd.. It received FDA 510(k) clearance on 2022-06-27 under 510(k) number K220309. 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 S10)?

Wearable Breast Pump (Model S10) is a medical device that received FDA 510(k) clearance on 2022-06-27. The listed applicant is Shenzhen Lutejiacheng Technology Co., Ltd.. The 510(k) number is K220309.

When did Wearable Breast Pump (Model S10) receive FDA 510(k) clearance?

Wearable Breast Pump (Model S10) received FDA 510(k) clearance on 2022-06-27, under 510(k) number K220309.

Who is the listed applicant for Wearable Breast Pump (Model S10)?

The FDA 510(k) record lists Shenzhen Lutejiacheng 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 S10)?

The FDA product code for Wearable Breast Pump (Model S10) is HGX.

列明Shenzhen Lutejiacheng Technology 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。

K230776Momcozy可穿戴电动吸奶器（型号：S9 Pro, S12 Pro）K223693电动吸奶器（型号：M5）

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。

K254203可穿戴式乳腺泵（型号S36）Shenzhen TPH Technology Co., Ltd.K261622飞利浦新安怡自然护理免手提电动吸奶器（型号：SCF593/52，SCF593/62）；飞利浦新安怡自然护理加热免手提电动吸奶器（型号：SCF594/52，SCF594/62）Philips Consumer Lifestyle B.V.K262774可穿戴式乳腺泵（型号：XN/MD-2249BS，ZFHF）Guangdong Horigen Mother & Baby Products Co., Ltd.K260643Cimilre 双重最大Cimilre Co., Ltd.K261298可穿戴电动吸奶器（YM-8837，YM-8838，YM-8856(H03)，YM-8809(S42)）Guangdong Youmeng Electrical Technology Co., Ltd.K260259DiscreetDuo™ 流动式穿戴型乳房吸奶器（型号 S3）Shenzhen TPH Technology Co., Ltd.

官方来源

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