meddevicedb.com FDA Device Reference

Sterisheet Sterilization Wrap

K170437 Class II Traditional
Decision Date
2017-11-01
Sponsor / Applicant
Andersen Sterilizers, Inc.

Technical Specification

510(k) Submission ID K170437
Product Code FRG
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6850
Decision Date 2017-11-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Sterisheet Sterilization Wrap received FDA 510(k) clearance under submission number K170437, sponsored by Andersen Sterilizers, 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 2017-11-01.

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.