meddevicedb.com FDA Device Reference

PILL PHONE

K060298 Class I Traditional
Decision Date
2006-03-29
Sponsor / Applicant
Vocel

Technical Specification

510(k) Submission ID K060298
Product Code NXQ
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5050
Decision Date 2006-03-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PILL PHONE received FDA 510(k) clearance under submission number K060298, sponsored by Vocel. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2006-03-29.

Classification & Regulation

This clearance is catalogued under FDA product code NXQ and 21 CFR 890.5050, within the Physical Medicine review panel as a Class I device.