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FDA 510(k)

Wearable Breast Pump (Model S1DW)

K-Number: K222045 · 2023-01-04

Decision Date2023-01-04
Product CodeHGX
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Wearable Breast Pump (Model S1DW) is a medical device manufactured by Shenzhen TPH Technology Co., Ltd.. It received FDA 510(k) clearance on 2023-01-04 under approval number K222045. 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 Wearable Breast Pump (Model S1DW)?

Wearable Breast Pump (Model S1DW) is a medical device that received FDA 510(k) clearance on 2023-01-04. It is manufactured by Shenzhen TPH Technology Co., Ltd.. The 510(k) number is K222045.

When was Wearable Breast Pump (Model S1DW) approved by the FDA?

Wearable Breast Pump (Model S1DW) received FDA 510(k) clearance on 2023-01-04, under approval number K222045.

What company makes Wearable Breast Pump (Model S1DW)?

Wearable Breast Pump (Model S1DW) is manufactured by Shenzhen TPH Technology Co., Ltd..

What is the FDA product code for Wearable Breast Pump (Model S1DW)?

The FDA product code for Wearable Breast Pump (Model S1DW) is HGX.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.