meddevicedb.com FDA Device Reference

STATVIEW SYSTEM

K990378 Class II Traditional
Decision Date
1999-09-20
Sponsor / Applicant
Data Critical Corp.

Technical Specification

510(k) Submission ID K990378
Product Code MSX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2300
Decision Date 1999-09-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STATVIEW SYSTEM received FDA 510(k) clearance under submission number K990378, sponsored by Data Critical Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1999-09-20.

Classification & Regulation

This clearance is catalogued under FDA product code MSX and 21 CFR 870.2300, within the Cardiovascular review panel as a Class II device.