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FDA 510(k)

Mosie Baby Kit

K-Number: K231203 · 2023-11-29

ApplicantMosie Baby
Decision Date2023-11-29
Product CodeQYZ
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Mosie Baby Kit is the device name listed in this FDA 510(k) record. The listed applicant is Mosie Baby. It received FDA 510(k) clearance on 2023-11-29 under 510(k) number K231203. The device is classified under product code QYZ. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Mosie Baby Kit?

Mosie Baby Kit is a medical device that received FDA 510(k) clearance on 2023-11-29. The listed applicant is Mosie Baby. The 510(k) number is K231203.

When did Mosie Baby Kit receive FDA 510(k) clearance?

Mosie Baby Kit received FDA 510(k) clearance on 2023-11-29, under 510(k) number K231203.

Who is the listed applicant for Mosie Baby Kit?

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

What is the FDA product code for Mosie Baby Kit?

The FDA product code for Mosie Baby Kit is QYZ.

Related Devices (Code: QYZ)

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.

K232579Twoplus ApplicatorHannah Life Technologies Pte , Ltd.K231645PherDal® At-Home Insemination KitPherdal Fertility Science, Inc.

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.

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