meddevicedb.com FDA Device Reference

VSM(R) R2 PAPER CHART RECORDER

K880554 Class I Traditional
Decision Date
1988-05-06
Sponsor / Applicant
Physio-Control Corp.

Technical Specification

510(k) Submission ID K880554
Product Code DSF
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2810
Decision Date 1988-05-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VSM(R) R2 PAPER CHART RECORDER received FDA 510(k) clearance under submission number K880554, 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 1988-05-06.

Classification & Regulation

This clearance is catalogued under FDA product code DSF and 21 CFR 870.2810, within the Cardiovascular review panel as a Class I device.