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FDA 510(k)

Momcozy Wearable Electric Breast Pump ( Model: S9 Pro, S12 Pro)

K-Number: K230776 · 2023-06-09

Decision Date2023-06-09
Product CodeHGX
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Momcozy Wearable Electric Breast Pump ( Model: S9 Pro, S12 Pro) is a medical device manufactured by Shenzhen Lutejiacheng Technology Co., Ltd.. It received FDA 510(k) clearance on 2023-06-09 under approval number K230776. 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 Momcozy Wearable Electric Breast Pump ( Model: S9 Pro, S12 Pro)?

Momcozy Wearable Electric Breast Pump ( Model: S9 Pro, S12 Pro) is a medical device that received FDA 510(k) clearance on 2023-06-09. It is manufactured by Shenzhen Lutejiacheng Technology Co., Ltd.. The 510(k) number is K230776.

When was Momcozy Wearable Electric Breast Pump ( Model: S9 Pro, S12 Pro) approved by the FDA?

Momcozy Wearable Electric Breast Pump ( Model: S9 Pro, S12 Pro) received FDA 510(k) clearance on 2023-06-09, under approval number K230776.

What company makes Momcozy Wearable Electric Breast Pump ( Model: S9 Pro, S12 Pro)?

Momcozy Wearable Electric Breast Pump ( Model: S9 Pro, S12 Pro) is manufactured by Shenzhen Lutejiacheng Technology Co., Ltd..

What is the FDA product code for Momcozy Wearable Electric Breast Pump ( Model: S9 Pro, S12 Pro)?

The FDA product code for Momcozy Wearable Electric Breast Pump ( Model: S9 Pro, S12 Pro) 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.