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BLOOD CARDIOPLEGIA HEAT EXCHANGER, MODEL #HE-30

K913956 Class II Traditional
Decision Date
1992-01-17
Sponsor / Applicant
Bentley Laboratories, Inc.

Technical Specification

510(k) Submission ID K913956
Product Code DTN
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4400
Decision Date 1992-01-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BLOOD CARDIOPLEGIA HEAT EXCHANGER, MODEL #HE-30 received FDA 510(k) clearance under submission number K913956, sponsored by Bentley Laboratories, 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 1992-01-17.

Classification & Regulation

This clearance is catalogued under FDA product code DTN and 21 CFR 870.4400, within the Cardiovascular review panel as a Class II device.