meddevicedb.com FDA Device Reference

POUCHES, GAS STERILIZATION

K781925 Class II Traditional
Decision Date
1978-11-22
Sponsor / Applicant
Medicare Industries, Inc.

Technical Specification

510(k) Submission ID K781925
Product Code FRG
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6850
Decision Date 1978-11-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

POUCHES, GAS STERILIZATION received FDA 510(k) clearance under submission number K781925, sponsored by Medicare Industries, Inc.. 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 1978-11-22.

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.