meddevicedb.com FDA Device Reference

Hypocore

K153162 Class II Traditional
Decision Date
2016-05-24
Sponsor / Applicant
Novocor Medical Systems, Inc.

Technical Specification

510(k) Submission ID K153162
Product Code NCX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.5900
Decision Date 2016-05-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Hypocore received FDA 510(k) clearance under submission number K153162, sponsored by Novocor Medical Systems, 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 2016-05-24.

Classification & Regulation

This clearance is catalogued under FDA product code NCX and 21 CFR 870.5900, within the Cardiovascular review panel as a Class II device.