meddevicedb.com FDA Device Reference

MEDI + FORM EXAM (MFG: GLOVE SEAL SDN BHD)

K893719 Class I Traditional
Decision Date
1989-09-13
Sponsor / Applicant
World Impex Corp.

Technical Specification

510(k) Submission ID K893719
Product Code LYY
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 1989-09-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDI + FORM EXAM (MFG: GLOVE SEAL SDN BHD) received FDA 510(k) clearance under submission number K893719, sponsored by World Impex Corp.. 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 1989-09-13.

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.