510(k) K041039

FERTELL MALE FERTILITY TEST by Genosis , Ltd. — Product Code POV

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 20, 2004
Date Received
April 22, 2004
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.