meddevicedb.com FDA Device Reference

SAFETY FIRST

K902708 Class I Traditional
Decision Date
1990-09-05
Sponsor / Applicant
Bright Rubber Industries Private , Ltd.

Technical Specification

510(k) Submission ID K902708
Product Code LYY
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 1990-09-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SAFETY FIRST received FDA 510(k) clearance under submission number K902708, sponsored by Bright Rubber Industries Private , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1990-09-05.

Classification & Regulation

This clearance is catalogued under FDA product code LYY and 21 CFR 880.6250, within the General Hospital review panel as a Class I device.