meddevicedb.com FDA Device Reference

AbStats Gateway

K150782 Class II Traditional
Decision Date
2015-12-14
Sponsor / Applicant
Gi Logic, Inc.

Technical Specification

510(k) Submission ID K150782
Product Code DQD
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1875
Decision Date 2015-12-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AbStats Gateway received FDA 510(k) clearance under submission number K150782, sponsored by Gi Logic, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2015-12-14.

Classification & Regulation

This clearance is catalogued under FDA product code DQD and 21 CFR 870.1875, within the Cardiovascular review panel as a Class II device.