meddevicedb.com FDA Device Reference

Level 1 Convective Warmer

K181699 Class II Traditional
Decision Date
2018-07-26
Sponsor / Applicant
Smiths Medical Asd, Inc.

Technical Specification

510(k) Submission ID K181699
Product Code DWJ
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.5900
Decision Date 2018-07-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Level 1 Convective Warmer received FDA 510(k) clearance under submission number K181699, sponsored by Smiths Medical Asd, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2018-07-26.

Classification & Regulation

This clearance is catalogued under FDA product code DWJ and 21 CFR 870.5900, within the Cardiovascular review panel as a Class II device.