510(k) K241628

YO Home Sperm Test by Medical Electronic Systems , Ltd. — Product Code POV

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 29, 2024
Date Received
June 6, 2024
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Semen Analysis Device
Device Class
Class II
Regulation Number
864.5220
Review Panel
HE
Submission Type

Device used to evaluate one or more human semen parameters including semen volume, sperm concentration, total sperm number, sperm motility, sperm morphology, sperm vitality, white blood cell concentration, and pH.