meddevicedb.com FDA Device Reference

SepaSperm Washing Solution, SepaSperm Solution

K190199 Class II Traditional
Decision Date
2019-09-26
Sponsor / Applicant
Kitazato Corporation

Technical Specification

510(k) Submission ID K190199
Product Code MQL
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.6180
Decision Date 2019-09-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SepaSperm Washing Solution, SepaSperm Solution received FDA 510(k) clearance under submission number K190199, sponsored by Kitazato Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 2019-09-26.

Classification & Regulation

This clearance is catalogued under FDA product code MQL and 21 CFR 884.6180, within the Obstetrics/Gynecology review panel as a Class II device.