meddevicedb.com FDA Device Reference

SELF-SEAL STERILIZATION POUCHES

K832128 Class II Traditional
Decision Date
1983-08-08
Sponsor / Applicant
Medical Industries Packaging, Inc.

Technical Specification

510(k) Submission ID K832128
Product Code KCT
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6850
Decision Date 1983-08-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SELF-SEAL STERILIZATION POUCHES received FDA 510(k) clearance under submission number K832128, sponsored by Medical Industries Packaging, 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 1983-08-08.

Classification & Regulation

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