Kidro Digital Electric Breast Pump, Dr. Brown's Digital Electric Breast Pump
K-Number: K192640 · 2020-03-30
Device Summary
Frequently Asked Questions
What is the Kidro Digital Electric Breast Pump, Dr. Brown's Digital Electric Breast Pump?
Kidro Digital Electric Breast Pump, Dr. Brown's Digital Electric Breast Pump is a medical device that received FDA 510(k) clearance on 2020-03-30. It is manufactured by Guangzhou Yongyi Industrial Co., Ltd.. The 510(k) number is K192640.
When was Kidro Digital Electric Breast Pump, Dr. Brown's Digital Electric Breast Pump approved by the FDA?
Kidro Digital Electric Breast Pump, Dr. Brown's Digital Electric Breast Pump received FDA 510(k) clearance on 2020-03-30, under approval number K192640.
What company makes Kidro Digital Electric Breast Pump, Dr. Brown's Digital Electric Breast Pump?
Kidro Digital Electric Breast Pump, Dr. Brown's Digital Electric Breast Pump is manufactured by Guangzhou Yongyi Industrial Co., Ltd..
What is the FDA product code for Kidro Digital Electric Breast Pump, Dr. Brown's Digital Electric Breast Pump?
The FDA product code for Kidro Digital Electric Breast Pump, Dr. Brown's Digital Electric Breast Pump is HGX.
Related Clinical Trials
Other Devices by Guangzhou Yongyi Industrial Co., Ltd.
Related Devices (Code: HGX)
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.