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NON-STERILE ORS WARNING DRAPES/SLUSH+WARMER DISC-DRAPE/SLUSH+WARMER PALTE-DRAPE /FLUID WARMER DRAPE,SKIRTED

K142080 Class I Special
Decision Date
2014-08-28
Sponsor / Applicant
Ecolab, Inc.

Technical Specification

510(k) Submission ID K142080
Product Code LHC
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5950
Decision Date 2014-08-28
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NON-STERILE ORS WARNING DRAPES/SLUSH+WARMER DISC-DRAPE/SLUSH+WARMER PALTE-DRAPE /FLUID WARMER DRAPE,SKIRTED received FDA 510(k) clearance under submission number K142080, sponsored by Ecolab, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2014-08-28.

Classification & Regulation

This clearance is catalogued under FDA product code LHC and 21 CFR 890.5950, within the Physical Medicine review panel as a Class I device.