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 a medical device manufactured by Willow Innovations, Inc.. It received FDA 510(k) clearance on 2022-02-09 under approval 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. It is manufactured by Willow Innovations, Inc.. The 510(k) number is K213311.

When was Lucy Breast Pump approved by the FDA?

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

What company makes Lucy Breast Pump?

Lucy Breast Pump is manufactured by Willow Innovations, Inc..

What is the FDA product code for Lucy Breast Pump?

The FDA product code for Lucy Breast Pump is HGX.

Other Devices by Willow Innovations, Inc.

K230570Willow Generation 3 Breast Pump

Related Devices (Code: HGX)

K162747Proture Double Electric Breast PumpGuangdong Horigen Mother & Baby Products Co., Ltd. K161725Sonata Breastpump Deluxe, Sonata Warranty Breastpump, Double pumping Tubing Kit, retail, Connector spare parts kit, Silicone Membrane, retail, Power Adaptor, retailMedela, Inc. K160274Hi bebe plusBistos Co., Ltd. K161532Philips Avent Comfort Single/Twin Electric Breast PumpPhilips Consumer Lifestyle - Innovation Site Eindhoven K161266Athena Breast PumpExploramed Nc7, Inc. K160511Naya Breast Pump SystemNaya Health, Inc.

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.