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KIMGUARD ONE-STEP Sterilization Wrap

K143053 Class II Traditional
Decision Date
2015-04-03
Sponsor / Applicant
Kimberly-Clark Health Care

Technical Specification

510(k) Submission ID K143053
Product Code FRG
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6850
Decision Date 2015-04-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

KIMGUARD ONE-STEP Sterilization Wrap received FDA 510(k) clearance under submission number K143053, sponsored by Kimberly-Clark Health Care. 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 2015-04-03.

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.