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FDA 510(k)

Lucy Breast Pump

K-Number: K213311 · 2022-02-09

Decision Date2022-02-09
Product CodeHGX
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Lucy Breast Pump is the device name listed in this FDA 510(k) record. The listed applicant is Willow Innovations, Inc.. It received FDA 510(k) clearance on 2022-02-09 under 510(k) number K213311. 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 Lucy Breast Pump?

Lucy Breast Pump is a medical device that received FDA 510(k) clearance on 2022-02-09. The listed applicant is Willow Innovations, Inc.. The 510(k) number is K213311.

When did Lucy Breast Pump receive FDA 510(k) clearance?

Lucy Breast Pump received FDA 510(k) clearance on 2022-02-09, under 510(k) number K213311.

Who is the listed applicant for Lucy Breast Pump?

The FDA 510(k) record lists Willow Innovations, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Lucy Breast Pump?

The FDA product code for Lucy Breast Pump is HGX.

Other records listing Willow Innovations, Inc. 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

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