meddevicedb.com FDA Device Reference

STERILIZATION TRAY LINER

K893764 Class II Traditional
Decision Date
1989-08-15
Sponsor / Applicant
Ahlstrom Dexter

Technical Specification

510(k) Submission ID K893764
Product Code FRG
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6850
Decision Date 1989-08-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STERILIZATION TRAY LINER received FDA 510(k) clearance under submission number K893764, sponsored by Ahlstrom Dexter. 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 1989-08-15.

Classification & Regulation

This clearance is catalogued under FDA product code FRG and 21 CFR 880.6850, within the General Hospital review panel as a Class II device.