FemaSeed Intratubal Insemination
K-Number: K231730 · 2023-09-22
ApplicantFemasys, Inc.
Decision Date2023-09-22
Product CodeMQF
Advisory CommitteeOB
DecisionSubstantially Equivalent
Device Summary
FemaSeed Intratubal Insemination is a medical device manufactured by Femasys, Inc.. It received FDA 510(k) clearance on 2023-09-22 under approval number K231730. The device is classified under product code MQF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the FemaSeed Intratubal Insemination?
FemaSeed Intratubal Insemination is a medical device that received FDA 510(k) clearance on 2023-09-22. It is manufactured by Femasys, Inc.. The 510(k) number is K231730.
When was FemaSeed Intratubal Insemination approved by the FDA?
FemaSeed Intratubal Insemination received FDA 510(k) clearance on 2023-09-22, under approval number K231730.
What company makes FemaSeed Intratubal Insemination?
FemaSeed Intratubal Insemination is manufactured by Femasys, Inc..
What is the FDA product code for FemaSeed Intratubal Insemination?
The FDA product code for FemaSeed Intratubal Insemination is MQF.
Other Devices by Femasys, Inc.
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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.