meddevicedb.com FDA Device Reference

BK-5203 FACILITATION VIBRATOR ELECTRIC

K800018 Class I Traditional
Decision Date
1980-01-21
Sponsor / Applicant
Fred Sammons, Inc.

Technical Specification

510(k) Submission ID K800018
Product Code IRO
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5975
Decision Date 1980-01-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BK-5203 FACILITATION VIBRATOR ELECTRIC received FDA 510(k) clearance under submission number K800018, sponsored by Fred Sammons, 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 1980-01-21.

Classification & Regulation

This clearance is catalogued under FDA product code IRO and 21 CFR 890.5975, within the Physical Medicine review panel as a Class I device.