meddevicedb.com FDA Device Reference

LIFESTAT 100

K853561 Class II Traditional
Decision Date
1986-06-09
Sponsor / Applicant
Physio-Control Corp.

Technical Specification

510(k) Submission ID K853561
Product Code DXN
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1130
Decision Date 1986-06-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LIFESTAT 100 received FDA 510(k) clearance under submission number K853561, 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 1986-06-09.

Classification & Regulation

This clearance is catalogued under FDA product code DXN and 21 CFR 870.1130, within the Cardiovascular review panel as a Class II device.