meddevicedb.com FDA Device Reference

Bead Block

K150876 Class II Traditional
Decision Date
2016-03-07
Sponsor / Applicant
Biocompatibles UK , Ltd.

Technical Specification

510(k) Submission ID K150876
Product Code KRD
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3300
Decision Date 2016-03-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Bead Block received FDA 510(k) clearance under submission number K150876, sponsored by Biocompatibles UK , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2016-03-07.

Classification & Regulation

This clearance is catalogued under FDA product code KRD and 21 CFR 870.3300, within the Cardiovascular review panel as a Class II device.