meddevicedb.com FDA Device Reference

CTS-3060 AUTOMATED SEMEN ANALYZER

K881765 Class II Traditional
Decision Date
1989-02-15
Sponsor / Applicant
Motion Analysis Corp.

Technical Specification

510(k) Submission ID K881765
Product Code POV
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.5220
Decision Date 1989-02-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CTS-3060 AUTOMATED SEMEN ANALYZER received FDA 510(k) clearance under submission number K881765, sponsored by Motion Analysis Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1989-02-15.

Classification & Regulation

This clearance is catalogued under FDA product code POV and 21 CFR 864.5220, within the Hematology review panel as a Class II device.