meddevicedb.com FDA Device Reference

CAS 740 SERIES MONITOR, MODELS 740-1, 740M-1, 740-2MS, 740M-2MS, 740-2NL, 740M-2NL, 740-2NN, 740M-2NN, 740-3MS, 740M-3MS

K033048 Class II Special
Decision Date
2004-06-01
Sponsor / Applicant
Cas Medical Systems, Inc.

Technical Specification

510(k) Submission ID K033048
Product Code MHX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1025
Decision Date 2004-06-01
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CAS 740 SERIES MONITOR, MODELS 740-1, 740M-1, 740-2MS, 740M-2MS, 740-2NL, 740M-2NL, 740-2NN, 740M-2NN, 740-3MS, 740M-3MS received FDA 510(k) clearance under submission number K033048, sponsored by Cas Medical Systems, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2004-06-01.

Classification & Regulation

This clearance is catalogued under FDA product code MHX and 21 CFR 870.1025, within the Cardiovascular review panel as a Class II device.