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APOLLO HEART RATE INDICATOR

K791207 Class II Traditional
Decision Date
1979-08-28
Sponsor / Applicant
Key Tronic Corp.

Technical Specification

510(k) Submission ID K791207
Product Code HCC
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5050
Decision Date 1979-08-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

APOLLO HEART RATE INDICATOR received FDA 510(k) clearance under submission number K791207, sponsored by Key Tronic Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1979-08-28.

Classification & Regulation

This clearance is catalogued under FDA product code HCC and 21 CFR 882.5050, within the Neurology review panel as a Class II device.