meddevicedb.com FDA Device Reference

STERIKING STERILIZATION POUCHES & ROLLS

K953776 Class II Traditional
Decision Date
1995-10-12
Sponsor / Applicant
Wihuri OY

Technical Specification

510(k) Submission ID K953776
Product Code KCT
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6850
Decision Date 1995-10-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STERIKING STERILIZATION POUCHES & ROLLS received FDA 510(k) clearance under submission number K953776, sponsored by Wihuri OY. 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 1995-10-12.

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.