meddevicedb.com FDA Device Reference

VITAL SIGNS MONITOR 2

K830587 Class II Traditional
Decision Date
1983-06-08
Sponsor / Applicant
Physio-Control Corp.

Technical Specification

510(k) Submission ID K830587
Product Code DRT
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2300
Decision Date 1983-06-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VITAL SIGNS MONITOR 2 received FDA 510(k) clearance under submission number K830587, sponsored by Physio-Control 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 1983-06-08.

Classification & Regulation

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