meddevicedb.com FDA Device Reference

Cardinal Health Sterilization Wrap

K181174 Class II Traditional
Decision Date
2018-12-11
Sponsor / Applicant
Cardinal Health200, LLC

Technical Specification

510(k) Submission ID K181174
Product Code FRG
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6850
Decision Date 2018-12-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Cardinal Health Sterilization Wrap received FDA 510(k) clearance under submission number K181174, sponsored by Cardinal Health200, LLC. 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 2018-12-11.

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.