meddevicedb.com FDA Device Reference

VSM-5

K852322 Class II Traditional
Decision Date
1985-09-11
Sponsor / Applicant
Physio-Control Corp.

Technical Specification

510(k) Submission ID K852322
Product Code DPS
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2340
Decision Date 1985-09-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VSM-5 received FDA 510(k) clearance under submission number K852322, 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 1985-09-11.

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.