FemaSeed Intratubal Insemination— 510(k) K231730
Substantially EquivalentFemasys, Inc.
FDA 510(k) clearance K231730 for FemaSeed Intratubal Insemination, Substantially Equivalent on 2023-09-22. Applicant: Femasys, Inc..
Clearance details
- Applicant
- Femasys, Inc.
- Product code
- Code MQF
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Suwanee, GA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.