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FDA 510(k)

Kidro Digital Electric Breast Pump, Dr. Brown's Digital Electric Breast Pump

K-Number: K192640 · 2020-03-30

Decision Date2020-03-30
Product CodeHGX
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Kidro Digital Electric Breast Pump, Dr. Brown's Digital Electric Breast Pump is a medical device manufactured by Guangzhou Yongyi Industrial Co., Ltd.. It received FDA 510(k) clearance on 2020-03-30 under approval number K192640. The device is classified under product code HGX. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

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

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Official Source

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