meddevicedb.com FDA Device Reference

SIME HEALTH SIME HYPOALLERGENIC

K931491 Class I Traditional
Decision Date
1993-10-15
Sponsor / Applicant
Sime Health, Ltd.

Technical Specification

510(k) Submission ID K931491
Product Code LYY
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 1993-10-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SIME HEALTH SIME HYPOALLERGENIC received FDA 510(k) clearance under submission number K931491, sponsored by Sime Health, 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 1993-10-15.

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.