meddevicedb.com FDA Device Reference

STOCKERT CAPS1 CARDIOPLEGIC CONTROL MODULE

K925661 Class II Traditional
Decision Date
1993-05-18
Sponsor / Applicant
Sorin Biomedica, Fiat, USA, Inc.

Technical Specification

510(k) Submission ID K925661
Product Code KRL
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4205
Decision Date 1993-05-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STOCKERT CAPS1 CARDIOPLEGIC CONTROL MODULE received FDA 510(k) clearance under submission number K925661, sponsored by Sorin Biomedica, Fiat, USA, 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 1993-05-18.

Classification & Regulation

This clearance is catalogued under FDA product code KRL and 21 CFR 870.4205, within the Cardiovascular review panel as a Class II device.