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FDA 510(k)

Annabella Double Breast Pump (ADO-US23-1000)

K-Number: K241506 · 2024-06-27

Decision Date2024-06-27
Product CodeHGX
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Annabella Double Breast Pump (ADO-US23-1000) is the device name listed in this FDA 510(k) record. The listed applicant is Annabella Tech. It received FDA 510(k) clearance on 2024-06-27 under 510(k) number K241506. 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 Annabella Double Breast Pump (ADO-US23-1000)?

Annabella Double Breast Pump (ADO-US23-1000) is a medical device that received FDA 510(k) clearance on 2024-06-27. The listed applicant is Annabella Tech. The 510(k) number is K241506.

When did Annabella Double Breast Pump (ADO-US23-1000) receive FDA 510(k) clearance?

Annabella Double Breast Pump (ADO-US23-1000) received FDA 510(k) clearance on 2024-06-27, under 510(k) number K241506.

Who is the listed applicant for Annabella Double Breast Pump (ADO-US23-1000)?

The FDA 510(k) record lists Annabella Tech as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Annabella Double Breast Pump (ADO-US23-1000)?

The FDA product code for Annabella Double Breast Pump (ADO-US23-1000) is HGX.

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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