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Sterisheet Sterilization Wrap

K152291 Class II Traditional
Decision Date
2015-12-17
Sponsor / Applicant
Andersen Sterilizers, Inc.

Technical Specification

510(k) Submission ID K152291
Product Code FRG
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6850
Decision Date 2015-12-17
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 K152291, 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 2015-12-17.

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.