meddevicedb.com FDA Device Reference

MINIATURIZE CHEST COMPRESSOR (MCC)

K102068 Class II Traditional
Decision Date
2010-11-16
Sponsor / Applicant
Resuscitation International

Technical Specification

510(k) Submission ID K102068
Product Code DRM
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.5200
Decision Date 2010-11-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MINIATURIZE CHEST COMPRESSOR (MCC) received FDA 510(k) clearance under submission number K102068, sponsored by Resuscitation International. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2010-11-16.

Classification & Regulation

This clearance is catalogued under FDA product code DRM and 21 CFR 870.5200, within the Cardiovascular review panel as a Class II device.