meddevicedb.com FDA Device Reference

MED-A-CALL ASSIST DEVICE

K890596 Class II Traditional
Decision Date
1989-03-14
Sponsor / Applicant
Silent Call Corp.

Technical Specification

510(k) Submission ID K890596
Product Code IQA
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3725
Decision Date 1989-03-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MED-A-CALL ASSIST DEVICE received FDA 510(k) clearance under submission number K890596, sponsored by Silent Call Corp.. 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 1989-03-14.

Classification & Regulation

This clearance is catalogued under FDA product code IQA and 21 CFR 890.3725, within the Physical Medicine review panel as a Class II device.