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TELEPHONE DEFIBRILLATOR SYSTEM

K864257 Class II Traditional
Decision Date
1987-11-27
Sponsor / Applicant
Medphone Corp.

Technical Specification

510(k) Submission ID K864257
Product Code LDD
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.5300
Decision Date 1987-11-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TELEPHONE DEFIBRILLATOR SYSTEM received FDA 510(k) clearance under submission number K864257, sponsored by Medphone 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 1987-11-27.

Classification & Regulation

This clearance is catalogued under FDA product code LDD and 21 CFR 870.5300, within the Cardiovascular review panel as a Class II device.