Lansinoh Signature Pro 双电动吸奶器，Lansinoh Smartpump 双电动吸奶器
K号: K182749 · 2019-06-12
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器械摘要
常见问题
What is the Lansinoh Signature Pro Double Electric Breast Pump, Lansinoh Smartpump Double Electric Breast Pump?
Lansinoh Signature Pro Double Electric Breast Pump, Lansinoh Smartpump Double Electric Breast Pump is a medical device that received FDA 510(k) clearance on 2019-06-12. The listed applicant is Lansinoh Laboratories Saglik Gerecleri Tasarim San. Tic., Ltd.. The 510(k) number is K182749.
When did Lansinoh Signature Pro Double Electric Breast Pump, Lansinoh Smartpump Double Electric Breast Pump receive FDA 510(k) clearance?
Lansinoh Signature Pro Double Electric Breast Pump, Lansinoh Smartpump Double Electric Breast Pump received FDA 510(k) clearance on 2019-06-12, under 510(k) number K182749.
Who is the listed applicant for Lansinoh Signature Pro Double Electric Breast Pump, Lansinoh Smartpump Double Electric Breast Pump?
The FDA 510(k) record lists Lansinoh Laboratories Saglik Gerecleri Tasarim San. Tic., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Lansinoh Signature Pro Double Electric Breast Pump, Lansinoh Smartpump Double Electric Breast Pump?
The FDA product code for Lansinoh Signature Pro Double Electric Breast Pump, Lansinoh Smartpump Double Electric Breast Pump is HGX.
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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。
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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