meddevicedb.com FDA Device Reference

CARECENTER MD

K093211 Class II Traditional
Decision Date
2010-06-03
Sponsor / Applicant
Cardiac Science Corporation

Technical Specification

510(k) Submission ID K093211
Product Code DPS
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2340
Decision Date 2010-06-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CARECENTER MD received FDA 510(k) clearance under submission number K093211, sponsored by Cardiac Science Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2010-06-03.

Classification & Regulation

This clearance is catalogued under FDA product code DPS and 21 CFR 870.2340, within the Cardiovascular review panel as a Class II device.