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PHOENIX SYSTEM SEVEN.

K862592 Class II Traditional
Decision Date
1986-09-16
Sponsor / Applicant
Nicolet Biomedical Instruments

Technical Specification

510(k) Submission ID K862592
Product Code EWO
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.1050
Decision Date 1986-09-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PHOENIX SYSTEM SEVEN. received FDA 510(k) clearance under submission number K862592, sponsored by Nicolet Biomedical Instruments. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 1986-09-16.

Classification & Regulation

This clearance is catalogued under FDA product code EWO and 21 CFR 874.1050, within the Ear, Nose, Throat review panel as a Class II device.