meddevicedb.com FDA Device Reference

HEART-CHILL SALINE SLUSH PAD

K882035 Class II Traditional
Decision Date
1988-07-28
Sponsor / Applicant
Buckman Co., Inc.

Technical Specification

510(k) Submission ID K882035
Product Code DWJ
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.5900
Decision Date 1988-07-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEART-CHILL SALINE SLUSH PAD received FDA 510(k) clearance under submission number K882035, sponsored by Buckman Co., 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 1988-07-28.

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.