meddevicedb.com FDA Device Reference

MODEL 405

K904606 Class II Traditional
Decision Date
1991-03-01
Sponsor / Applicant
Ivy Biomedical Systems, Inc.

Technical Specification

510(k) Submission ID K904606
Product Code DPS
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2340
Decision Date 1991-03-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODEL 405 received FDA 510(k) clearance under submission number K904606, sponsored by Ivy Biomedical 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 1991-03-01.

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.