meddevicedb.com FDA Device Reference

Xprecia Stride Coagulation System, Xprecia System PT Controls

K151964 Class II Traditional
Decision Date
2016-09-30
Sponsor / Applicant
Siemens Healthcare Diagnostics

Technical Specification

510(k) Submission ID K151964
Product Code GJS
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.7750
Decision Date 2016-09-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Xprecia Stride Coagulation System, Xprecia System PT Controls received FDA 510(k) clearance under submission number K151964, sponsored by Siemens Healthcare Diagnostics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 2016-09-30.

Classification & Regulation

This clearance is catalogued under FDA product code GJS and 21 CFR 864.7750, within the Hematology review panel as a Class II device.