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KIMGUARD ONE STEP STERILIZATION WRAP

K141712 Class II Traditional
Decision Date
2014-12-18
Sponsor / Applicant
Halyard Health

Technical Specification

510(k) Submission ID K141712
Product Code FRG
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6850
Decision Date 2014-12-18
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 K141712, sponsored by Halyard Health. 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 2014-12-18.

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.