meddevicedb.com FDA Device Reference

COMMUNI-CALL

K893473 Class II Traditional
Decision Date
1989-06-09
Sponsor / Applicant
Carepartners, Inc.

Technical Specification

510(k) Submission ID K893473
Product Code ILQ
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3710
Decision Date 1989-06-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COMMUNI-CALL received FDA 510(k) clearance under submission number K893473, sponsored by Carepartners, Inc.. 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 1989-06-09.

Classification & Regulation

This clearance is catalogued under FDA product code ILQ and 21 CFR 890.3710, within the Physical Medicine review panel as a Class II device.