meddevicedb.com FDA Device Reference

SELF SEAL STERILIZATION POUCH

K071886 Class II Traditional
Decision Date
2007-12-27
Sponsor / Applicant
Shanghai Jianzhong Medical Packaging Co., Ltd.

Technical Specification

510(k) Submission ID K071886
Product Code FRG
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6850
Decision Date 2007-12-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SELF SEAL STERILIZATION POUCH received FDA 510(k) clearance under submission number K071886, sponsored by Shanghai Jianzhong Medical Packaging Co., 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 2007-12-27.

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.