Wearable Breast Pump (Model S12)
K-Number: K212180 · 2022-02-11
Device Summary
Frequently Asked Questions
What is the Wearable Breast Pump (Model S12)?
Wearable Breast Pump (Model S12) is a medical device that received FDA 510(k) clearance on 2022-02-11. The listed applicant is Shenzhen TPH Technology Co., Ltd.. The 510(k) number is K212180.
When did Wearable Breast Pump (Model S12) receive FDA 510(k) clearance?
Wearable Breast Pump (Model S12) received FDA 510(k) clearance on 2022-02-11, under 510(k) number K212180.
Who is the listed applicant for Wearable Breast Pump (Model S12)?
The FDA 510(k) record lists Shenzhen TPH 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 S12)?
The FDA product code for Wearable Breast Pump (Model S12) is HGX.
Other records listing Shenzhen TPH Technology Co., Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: HGX)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.