meddevicedb.com FDA Device Reference

SORBA MODEL CIC-1000 NON-INVASIVE HEMODYNAMIC MONITOR

K950389 Class II Traditional
Decision Date
1995-08-15
Sponsor / Applicant
Sorba Medical Systems, Inc.

Technical Specification

510(k) Submission ID K950389
Product Code DSB
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2770
Decision Date 1995-08-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SORBA MODEL CIC-1000 NON-INVASIVE HEMODYNAMIC MONITOR received FDA 510(k) clearance under submission number K950389, sponsored by Sorba Medical Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1995-08-15.

Classification & Regulation

This clearance is catalogued under FDA product code DSB and 21 CFR 870.2770, within the Cardiovascular review panel as a Class II device.